Who is the manufacturer of Sterilization Tray?

STERIS Corporation filed the 510(k) submission for Sterilization Tray (K160912).

What is the FDA product code for Sterilization Tray?

KCT. It is classified under 21 CFR 880.6850 as a Class 2 device in the General Hospital panel.

What is the regulatory pathway for Sterilization Tray?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like Sterilization Tray?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Sterilization Tray

Q: What are the predicate devices for Sterilization Tray?

V-PRO Sterilization Tray (K140494).

K160912 · STERIS Corporation · KCT · Oct 7, 2016 · General Hospital

Device Facts

Record ID	K160912
Device Name	Sterilization Tray
Applicant	STERIS Corporation
Product Code	KCT · General Hospital
Decision Date	Oct 7, 2016
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 880.6850
Device Class	Class 2

Intended Use

The Sterilization Trays are used to contain medical devices for sterilization in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems. Prior to placing in the Sterilizer, the trays must either be: - wrapped with a legally marketed sterilization wrap for use in the V-PRO Low Temperature Sterilization Systems or - placed inside a legally marketed pouch for enclosing trays in the V-PRO Low Temperature Sterilization Systems. The Sterilization Trays are not intended to maintain sterility; they are intended to be used in conjunction with a validated, FDA-cleared sterilization wrap or pouch in order to maintain sterility of the enclosed medical instruments.

Device Story

Sterilization trays contain medical devices (endoscopes, forceps, scissors) for processing in V-PRO Low Temperature Sterilization Systems. Trays feature base and lid with clamping mechanisms and perforations for sterilant penetration. Accessories include silicone instrument organizers and mats to cushion/stabilize devices. Used in clinical settings by healthcare staff. Trays must be enclosed in FDA-cleared sterilization wrap or pouch; they do not maintain sterility independently. Output is a sterilized instrument load ready for storage/use. Benefits include protection of delicate instruments and validated sterilization of diffusion-restricted spaces (lumens/hinges).

Clinical Evidence

Bench testing only. Studies included effective sterilant penetration, drying/aeration (hydrogen peroxide residuals), cleaning efficacy, material compatibility, and biocompatibility (cytotoxicity) under worst-case sterilization cycle conditions. No clinical data.

Technological Characteristics

Materials: Glass-filled polypropylene, stainless steel, and medical-grade silicone (USP grade VI). Design: Perforated base/lid with clamping mechanism. Dimensions: Various sizes (13x4.5x2.25 to 25x14x5 inches). Connectivity: None. Sterilization: V-PRO Low Temperature Sterilization Systems. No software/algorithm.

Indications for Use

Indicated for containing medical devices, including rigid/semi-rigid/flexible endoscopes, forceps, and scissors, during sterilization in V-PRO Low Temperature Sterilization Systems. Patient population includes those undergoing procedures requiring sterilized surgical instruments; no specific age or gender restrictions.

Regulatory Classification

Identification

A sterilization wrap (pack, sterilization wrapper, bag, or accessories, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used.

Predicate Devices

V-PRO Sterilization Tray (K140494)

Related Devices

K172755 — PRO-LITE Sterilization Trays · STERIS Corporation · Feb 9, 2018
K140494 — V-PRO STERILIZATION TRAY/ STERILIZATION MAT · STERIS Corporation · Jul 25, 2014
K183402 — PRO-LITE Sterilization Tray · STERIS Corporation · Mar 1, 2019
K070769 — VHP 136 TRAY · STERIS Corporation · Oct 5, 2007
K183301 — PRO-LITE Sterilization Tray · STERIS Corporation · Jan 3, 2019

Submission Summary (Full Text)

{0}------------------------------------------------ Image /page/0/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a circular seal with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is an abstract symbol that resembles a stylized caduceus or a series of human profiles. Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 October 7, 2016 STERIS Corporation Mr. Tony Piotrkowski Senior Manager, Regulatory Affairs 5960 Heisley Road Mentor, OH 44060 Re: K160912 Trade/Device Name: Sterilization Tray Regulation Number: 21 CFR 880.6850 Regulation Name: Sterilization Wrap Regulatory Class: Class II Product Code: KCT Dated: September 9, 2016 Received: September 12, 2016 Dear Mr. Tony Piotrkowski : We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food. Drug. and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading. If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801 and Part 809); medical device reporting (reporting of {1}------------------------------------------------ medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and Part 809), please contact the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to http://www.fda.gov/MedicalDevices/Safety/ReportaProblem/default.htm for the CDRH's Office of Surveillance and Biometrics/Division of Postmarket Surveillance. You may obtain other general information on your responsibilities under the Act from the Division of Industry and Consumer Education at its toll-free number (800) 638-2041 or (301) 796-7100 or at its Internet address http://www.fda.gov/MedicalDevices/ResourcesforYou/Industry/default.htm. Sincerely yours. # Michael J. Ryan -S for Tina Kiang, Ph.D. Acting Director Division of Anesthesiology, General Hospital, Respiratory, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ # DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration # Indications for Use 510(k) Number (if known) Device Name Sterilization Trays K160912 # Indications for Use (Describe) The Sterilization Trays are used to contain medical devices for sterilization in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems. Prior to placing in the Sterilizer, the trays must either be: - wrapped with a legally marketed sterilization wrap for use in the V-PRO Low Temperature Sterilization Systems ● or - placed inside a legally marketed pouch for enclosing trays in the V-PRO Low Temperature Sterilization Systems. The Sterilization Trays are not intended to maintain sterility; they are intended to be used in conjunction with a validated, FDA-cleared sterilization wrap or pouch in order to maintain sterility of the enclosed medical instruments. | Model Number (size LxWxH in inches) | Intended Sterilization Cycles | Intended Tray Load | |----------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | VP0045 (13x4.5x2.25) VP0046 (19x4.5x2.25) VP0047 (25x4.5x2.25) VP0048 (13x7.75x2.25) VP0049 (19x7.75x2.25) VP0050 (27x7.75x4) | V-PRO 60 Lumen Cycle | • Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors • Non-lumened devices including non-lumened rigid and semi-rigid endoscopes • Medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations: o single or dual lumen devices ▪ ≥ 0.77 mm ID and ≤ 410 mm in length o triple lumen devices ▪ ≥1.2 mm ID and ≤ 275 mm in length ▪ ≥1.8 mm ID and ≤ 310 mm in length or ▪ ≥2.8 mm ID and ≤ 317 mm in length | | | V-PRO 60 Non Lumen Cycle | Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel or titanium diffusion-restricted spaces such as the hinged portion of forceps and scissors. | | VP0045 (13x4.5x2.25) VP0046 (19x4.5x2.25) VP0047 (25x4.5x2.25) VP0048 (13x7.75x2.25) VP0049 (19x7.75x2.25) VP0050 (27x7.75x4) | V-PRO 60 Flexible Cycle | One flexible surgical endoscope or bronchoscope with a light cord (if not integral to endoscope) and mat without any additional load. The flexible endoscope may be a single or dual lumen device with lumens that are ≥ 1 mm ID and ≤ 990 mm in length | | VP0051 (12x11.75x4) VP0052 (25x11,75x4.5) VP0053 (25x14x5) | V-PRO 1, 1 Plus & maX Lumen Cycle | • Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors • Non-lumened devices including non-lumened rigid and semi-rigid endoscopes • Medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations: o single or dual lumen devices ▪ ≥ 0.77 mm ID and ≤ 527 mm in length o triple lumen devices ▪ ≥ 1.2 mm ID and ≤ 275 mm in length ▪ ≥ 1.8 mm ID and ≤ 310 mm in length or ▪ ≥ 2.8 mm ID and ≤ 317 mm in length | | | V-PRO 1 Plus & maX Non Lumen Cycle | Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel diffusion-restricted spaces such as the hinged portion of forceps and scissors. | {3}------------------------------------------------ | Model Number (size LxWxH in inches) | Intended Sterilization Cycles | Intended Tray Load | |------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | VP0045 (13x4.5x2.25) VP0046 (19x4.5x2.25) VP0047 (25x4.5x2.25) VP0048 (13x7.75x2.25) VP0049 (19x7.75x2.25) VP0050 (27x7.75x4) VP0051 (12x11.75x4) VP0052 (25x11.75x4.5) VP0053 (25x14x5) | V-PRO maX Flexible Cycle | Load 1: Single or dual lumen surgical flexible endoscopes (such as those used in ENT, Urology and Surgical Care) and bronchoscopes with a light cord (if not integral to endoscope) and mat with no additional load. The flexible endoscopes may contain either: • a single lumen that is ≥ 1 mm ID and ≤ 1050 mm in length • or two lumens with: • one lumen that is ≥ 1 mm ID and ≤ 990 mm in length • and the other lumen that is ≥ 1 mm ID and ≤ 850 mm in length Load 2: Non-lumened instruments including instruments with diffusion-restricted areas such as the hinged portion of forceps or scissors. | Instrument organizers are optional accessories intended to stabilize cylindrical instruments within the Sterilization Trays. | Model | Description | Model | Description | |--------|---------------------|--------|----------------------| | VP0063 | 3 mm - 7 mm, Tall | VP0067 | 3 mm - 7 mm, Short | | VP0064 | 7 mm - 11 mm, Tall | VP0068 | 7 mm - 11 mm, Short | | VP0065 | 11 mm - 15 mm, Tall | VP0069 | 11 mm - 15 mm, Short | | VP0066 | 15 mm - 19 mm, Tall | VP0070 | 15 mm - 19 mm, Short | Sterilization mats are optional accessories intended to cushion and stabilize instruments within the Sterilization Trays. | Model | Description | Model | Description | Model | Description | |--------|-------------|--------|-------------|--------|-------------| | VP0071 | 13 x 4.5 | VP0074 | 13 x 7.75 | VP0077 | 12 x 11.75 | | VP0072 | 19 x 4.5 | VP0075 | 19 x 7.75 | VP0078 | 25 x 11.75 | | VP0073 | 25 x 4.5 | VP0076 | 27 x 7.75 | VP0079 | 25 x 14 | Type of Use (Select one or both, as applicable) | Prescription Use (Part 21 CFR 801 Subpart D) | X Over-The-Counter Use (21 CFR 801 Subpart C) # CONTINUE ON A SEPARATE PAGE IF NEEDED. This section applies only to requirements of the Paperwork Reduction Act of 1995. # *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.* The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to: > Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff(@fda.hhs.gov "An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number." FORM FDA 3881 (8/14) EF {4}------------------------------------------------ # STERIS® # 510(k) Summary For Sterilization Trays # Sponsor Facility STERIS Corporation 5960 Heisley Road Mentor, OH 44060 Phone: (440) 354-2600 Fax No: (440) 357-9198 # Repackager/Relabeler Facility STERIS Corporation 9325 Pinecone Drive Mentor, OH 44060 Phone: (440) 392-7800 Fax No: (440) 392-7896 Contact: Tony Piotrkowski Senior Manager, Regulatory Affairs Telephone: (440) 392-7437 Fax No: (440) 357-9198 e-mail: tpiotrko@steris.com Submission Date: September 9, 2016 STERIS Corporation ■ 5960 Heisley Road ■ Mentor, OH 44060-1834 USA ■ 440-354-2600 {5}------------------------------------------------ # K160912/S001 STERIS Response to 5/31/16 Request for Additional Information Sterilization Travs ### Device Name 1. | Trade Name: | Sterilization Trays | |----------------------|-----------------------------------------------------------------------| | Common/usual Name: | Sterilization Trays, cassettes and other accessories | | Classification Name: | Sterilization Wrap 21 CFR 880.6850 Class II Product Code KCT | ### Predicate Device 2. V-PRO Sterilization Tray K140494 ### 3. Description of Device The Sterilization Trays contain medical devices for sterilization in the V-PRO Low Temperature Sterilization Systems: V-PRO 1, V-PRO 1 Plus, V-PRO maX and V-PRO 60 Low Temperature Sterilization Systems. The trays are available in various sizes, outlined in Table 10-1, to accommodate the loads to be processed. The proposed trays are similar in design to the predicate V-PRO Sterilization Tray (K140494) and are composed of a base and a lid. The lid includes clamping mechanisms designed to secure the lid onto the base. There are numerous holes in the base and lid for sterilant penetration. The tray is categorized as a cassette and requires complete enclosure in a legally-marketed sterilization wrap or pouch to maintain sterility of the enclosed devices. | Model | Description | Model | Description | |--------|------------------|--------|------------------| | VP0045 | 13 x 4.5 x 2.25 | VP0050 | 27 x 7.75 x 4 | | VP0046 | 19 x 4.5 x 2.25 | VP0051 | 12 x 11.75 x 4 | | VP0047 | 25 x 4.5 x 2.25 | VP0052 | 25 x 11.75 x 4.5 | | VP0048 | 13 x 7.75 x 2.25 | VP0053 | 25 x 14 x 5 | | VP0049 | 19 x 7.75 x 2.25 | | | Table 10-1. External Dimensions of Tray Line Optional instrument organizers are provided as accessories to the trays and allow stabilization of various cylindrical medical devices during processing. Table 10-2 lists the organizer sizes. The organizers are either "blank" and are used to partition the tray or have a device holding portion into which the devices are inserted. At the organizer base is a flapped groove that is used to position the organizer within a Sterilization Tray. {6}------------------------------------------------ | Model | Description | Model | Description | |--------|---------------------|--------|----------------------| | VP0063 | 3 mm - 7mm, Tall | VP0067 | 3 mm - 7 mm, Short | | VP0064 | 7 mm - 11mm, Tall | VP0068 | 7 mm -11 mm, Short | | VP0065 | 11 mm - 15 mm, Tall | VP0069 | 11 mm - 15 mm, Short | | VP0066 | 15 mm - 19mm, Tall | VP0070 | 15 mm - 19 mm, Short | # K160912/S001 STERIS Response to 5/31/16 Request for Additional Information Sterilization Travs Optional sterilization mats are provided as accessories to the trays. The mats, which are used to cushion and stabilize devices placed into the trays, are available in sizes as shown in Table 10-3 to fit the nine Sterilization Trays. The mats are a diamond grid design with "fingers" that extend from each corner of the diamond and at the midpoint of each diamond side. The fingers cushion and stabilize instruments, helping to prevent the instruments from freely moving in the tray during packaging, sterilization and storage. The cushioning and stabilization qualities help protect delicate instruments placed into the trays. Table 10-3. Sterilization Tray Model Numbers | Model | Description | Model | Description | |--------|-------------|--------|-------------| | VP0071 | 13 x 4.5 | VP0076 | 27 x 7.75 | | VP0072 | 19 x 4.5 | VP0077 | 12 x 11.75 | | VP0073 | 25 x 4.5 | VP0078 | 25 x 11.75 | | VP0074 | 13 x 7.75 | VP0079 | 25 x 14 | | VP0075 | 19 x 7.75 | | | ### 4. Intended Use/ Indications for Use The Sterilization Trays are used to contain medical devices for sterilization in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems. Prior to placing in the Sterilizer, the trays must either be: - . wrapped with a legally marketed sterilization wrap for use in the V-PRO Low Temperature Sterilization Systems or - . placed inside a legally marketed pouch for enclosing trays in the V-PRO Low Temperature Sterilization Systems. The Sterilization Trays are not intended to maintain sterility; they are intended to be used in conjunction with a validated, FDA-cleared sterilization wrap or pouch in order to maintain sterility of the enclosed medical instruments. {7}------------------------------------------------ # K160912/S001 STERIS Response to 5/31/16 Request for Additional Information Sterilization Trays | Model Number (size LxWxH in inches) | Intended Sterilization Cycles | Intended Tray Load | |------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | | V-PRO 60 Lumen Cycle | • Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors • Non-lumened devices including non-lumened rigid and semi- rigid endoscopes • Medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations: o single or dual lumen devices • ≥ 0.77 mm ID and ≤ 410 mm in length o triple lumen devices • ≥1.2 mm ID and ≤ 275 mm in length • ≥1.8 mm ID and ≤ 310 mm in length or • ≥2.8 mm ID and ≤ 317 mm in length | | VP0045 (13x4.5x2.25) VP0046 (19x4.5x2.25) VP0047 (25x4.5x2.25) VP0048 (13x7.75x2.25) VP0049 (19x7.75x2.25) VP0050 (27x7.75x4) VP0051 (12x11.75x4) VP0052 (25x11,75x4.5) VP0053 (25x14x5) | V-PRO 60 Non Lumen Cycle | Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel or titanium diffusion-restricted spaces such as the hinged portion of forceps and scissors. | | | V-PRO 60 Flexible Cycle | One flexible surgical endoscope or bronchoscope with a light cord (if not integral to endoscope) and mat without any additional load. The flexible endoscope may be a single or dual lumen device with lumens that are > 1 mm ID and < 990 mm in length | | | V-PRO 1, 1 Plus & maX Lumen Cycle | • Instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors • Non-lumened devices including non-lumened rigid and semi- rigid endoscopes • Medical devices, including single, dual and triple channeled rigid and semi-rigid endoscopes, with the following configurations: o single or dual lumen devices • ≥ 0.77 mm ID and ≤ 527 mm in length o triple lumen devices • ≥ 1.2 mm ID and ≤ 275 mm in length • ≥ 1.8 mm ID and ≤ 310 mm in length or • ≥ 2.8 mm ID and ≤ 317 mm in length | | | V-PRO 1 Plus & maX Non Lumen Cycle | Non-lumened devices including non-lumened rigid, semi-rigid and flexible endoscopes and non-lumened devices with stainless steel diffusion-restricted spaces such as the hinged portion of forceps and scissors. | | Model Number (size LxWxH in inches) | Intended Sterilization Cycles | Intended Tray Load | | VP0045 (13x4.5x2.25) VP0046 (19x4.5x2.25) VP0047 (25x4.5x2.25) VP0048 (13x7.75x2.25) VP0049 (19x7.75x2.25) VP0050 (27x7.75x4) VP0051 (12x11.75x4) VP0052 (25x11.75x4.5) VP0053 (25x14x5) | V-PRO maX Flexible Cycle | Load 1: Single or dual lumen surgical flexible endoscopes (such as those used in ENT, Urology and Surgical Care) and bronchoscopes with a light cord (if not integral to endoscope) and mat with no additional load. The flexible endoscopes may contain either: a single lumen that is ≥ 1 mm ID and ≤ 1050 mm in length or two lumens with: one lumen that is ≥ 1 mm ID and ≤ 990 mm in length and the other lumen that is ≥ 1 mm ID and ≤ 850 mm in length Load 2: Non-lumened instruments including instruments with diffusion-restricted areas such as the hinged portion of forceps or scissors. | {8}------------------------------------------------ # K160912/S001 STERIS Response to 5/31/16 Request for Additional Information Sterilization Trays Instrument organizers are optional accessories intended to stabilize cylindrical medical instruments within the Sterilization Trays. | Model | Description | Model | Description | |--------|---------------------|--------|----------------------| | VP0063 | 3 mm - 7mm, Tall | VP0067 | 3 mm - 7 mm, Short | | VP0064 | 7 mm - 11mm, Tall | VP0068 | 7 mm - 11 mm, Short | | VP0065 | 11 mm - 15 mm, Tall | VP0069 | 11 mm - 15 mm, Short | | VP0066 | 15 mm - 19mm, Tall | VP0070 | 15 mm - 19 mm, Short | Sterilization mats are optional accessories intended to cushion and stabilize instruments within the Sterilization Trays. | Model | Description | Model | Description | Model | Description | |--------|-------------|--------|-------------|--------|-------------| | VP0071 | 13 x 4.5 | VP0074 | 13 x 7.75 | VP0077 | 12 x 11.75 | | VP0072 | 19 x 4.5 | VP0075 | 19 x 7.75 | VP0078 | 25 x 11.75 | | VP0073 | 25 x 4.5 | VP0076 | 27 x 7.75 | VP0079 | 25 x 14 | ### ട്. Summary of Technical Characteristics The sterilization trays, sterilization mats and instrument organizers are identical in composition to the claimed predicate devices. The technical characteristics are summarized in Table 10-4. {9}------------------------------------------------ | Feature | Sterilization Tray (proposed) | V-PRO Sterilization Tray (K140494) | Comparison | |----------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Intended Use | The Sterilization Trays are used to contain medical devices for sterilization in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems. Prior to placing in the Sterilizer, the trays must either be: • wrapped with a legally marketed sterilization wrap for use in the V-PRO Low Temperature Sterilization Systems or • placed inside a legally marketed pouch for enclosing trays in the V-PRO Low Temperature Sterilization Systems. The Sterilization Trays are not intended to maintain sterility; they are intended to be used in conjunction with a validated, FDA-cleared sterilization wrap or pouch in order to maintain sterility of the enclosed medical instruments. Instrument organizers are optional accessories intended to stabilize cylindrical medical instruments within the Sterilization Trays. Sterilization mats are optional accessories intended to cushion and stabilize instruments within the Sterilization Trays. | The V-PRO Sterilization Tray is used to contain medical devices for sterilization in the Lumen, Non Lumen and Flexible Cycles of the V-PRO Low Temperature Sterilization Systems and to maintain sterility of properly processed medical devices during normal handling and storage until they are removed for use. The trays must be wrapped with a legally marketed sterilization wrap for use in the V-PRO Low Temperature Sterilization Systems prior to placing in the Sterilizer. Optional instrument organizers are accessories to the tray and are intended to allow stabilization of various cylindrical medical devices during processing. The instrument organizers attach to the V-PRO Sterilization Tray base and stabilize cylindrical medical instruments. | Adding ability to pouch trays for sterilization or to process pouched items in a wrapped or pouched tray - peroxide residual and sterilant penetration testing demonstrate safety and efficacy. Use of Vis-U-All pouches with the trays is part of separate, concurrent, submission. | | Vent to Volume Ratio | All trays are the same: 0.135 in-1 | All trays are the same: 0.137 in-1 | Similar; peroxide residual and sterilant penetration testing demonstrate safety and efficacy | | Tray Composition | Glass-filled polypropylene, stainless steel | Polypropylene, Noryl and stainless steel | Similar, Compatibility testing demonstrates safety and efficacy | | Feature | Sterilization Tray (proposed) | V-PRO Sterilization Tray (K140494) | Comparison | | Organizer Composition | Medical Grade Silicone, USP grade VI | Polypropylene | Compatibility testing demonstrates safety and efficacy | | Mat Composition | Medical Grade Silicone, USP grade VI | Medical Grade Silicone, USP grade VI | Same | # Table 10-4 Summary of Tray Physical Description and Technological Properties {10}------------------------------------------------ # K160912/S001 STERIS Response to 5/31/16 Request for Additional Information Sterilization Trays ### Summary of Nonclinical Tests 6. Performance testing to demonstrate substantial equivalence to the predicate has been completed and is summarized in Table 10-5 below. | Test | Acceptance Criteria | Conclusion | |----------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------|------------| | Demonstration of Effective Sterilant Penetration | Worst case test article packaged in the trays shall be reproducibly sterilized under worst case ½ cycle conditions. | PASS | | Package Integrity Maintenance of Package Integrity | Not applicable, Trays to be used with legally marketed sterilization wrap or pouch. | | | Demonstration of Effective Drying and Aeration | Residual hydrogen peroxide levels shall be below acceptable levels after exposure to worst case Sterilizer Cycle conditions. | PASS | | Demonstration of Effective Cleaning | Clean following automated and manual cleaning. | PASS | | Demonstration of Material Compatibility | After processing through multiple worst case sterilization cycles, the trays and accessories shall retain functionality. | PASS | | Demonstration of Biocompatibility | Component materials shall be non cytotoxic after exposure to worst case Sterilizer Cycle conditions. | PASS | # Table 10-5. Summary of Non-clinical Testing ### 7. Conclusion The Sterilization Trays have met the established performance criteria. The results of the studies demonstrate that the sterilization trays and accessories perform as intended, and based on the nonclinical tests performed, the subject device is as safe, as effective, and performs at least as safely and effectively as the legally marketed predicate devices, Class II (21 CFR 880.6850, Product code KCT.