SECURELOC; ADVANCINTRODUCER
Device Facts
| Record ID | K050023 |
|---|---|
| Device Name | SECURELOC; ADVANCINTRODUCER |
| Applicant | Specialized Health Products, Inc. |
| Product Code | DYB · Cardiovascular |
| Decision Date | Feb 18, 2005 |
| Decision | SESE |
| Submission Type | Traditional |
| Regulation | 21 CFR 870.1340 |
| Device Class | Class 2 |
Indications for Use
Both the AdvancIntroducer™ and the SecureLoc™ Safety Introducer Needles are intended to be used for those patients requiring percutaneous procedures utilizing an introducer needle for guidewire placement for subsequent placement of catheters or other introducer needle required medical procedures. The SecureLoc™ Safety Introducer Needle's safety engineered integral safety guard is advanced by the clinician. The safety guard automatically senses the end of the needle and locks covering the needle tip. The SecureLoc™ Safety Introducer Needle's easy to use intuitive safety guard reduces the risk of accidental needlestick injuries by shielding the needle point. The safety guard can be activated over stylettes, obturators, and guidewires. The AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles will be marketed as both bulk non-sterile single use devices to procedural kit manufacturers and also as sterile, non-pyrogenic, single use devices to clinical end-users. The AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles may be used in any appropriate patient population.
Device Story
AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles facilitate percutaneous guidewire placement for catheterization. Devices consist of stainless steel needle, Luer lock hub, and optional echogenic features/coatings. SecureLoc™ includes integral safety guard; clinician-advanced post-procedure to shield needle tip; provides visual, tactile, and audible confirmation of lockout. Used in clinical settings by healthcare providers; also supplied as bulk components for procedural kits. Safety guard prevents accidental needlestick injuries; remains locked through disposal. Benefits include improved ergonomic stability and reduced sharps injury risk.
Clinical Evidence
Bench testing and simulated use study performed. 500 SecureLoc™ needles tested in simulated tissue by clinicians; 100% success rate in activation; zero sharps injuries or mechanical failures of the safety guard reported.
Technological Characteristics
Stainless steel needle; translucent Luer lock hub; optional echogenic features/coatings. Manual safety guard mechanism; integral to device. Single-use; sterile or bulk non-sterile. No electronic components or software.
Indications for Use
Indicated for patients requiring percutaneous procedures utilizing an introducer needle for guidewire placement for subsequent catheter or other medical device placement. No specific age or gender restrictions; may be used in any appropriate patient population.
Regulatory Classification
Identification
A catheter introducer is a sheath used to facilitate placing a catheter through the skin into a vein or artery.
Predicate Devices
- Safety Introducer Needles (K030135)
- Majestik™ Angiographic Introducer Needles (pre-amendment)
Submission Summary (Full Text)
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K050023
FEB 1 8 2005
Lot 3
# 510(k) SUMMARY OF SAFETY AND EFFECTIVENESS (21 CFR 807.92) for the SecureLoc™Safety Introducer Needles
## SUBMITTER:
Specialized Health Products®, Inc. 585 West 500 South, Suite 200 Bountiful, Utah 84010
## ESTABLISHMENT REGISTRATION NUMBER: 1723684
## CONTACT:
Mark Nelson Director, Quality and Regulatory Affairs Telephone: 801-298-3360 Fax: 801-298-1759 Email: marknelson@shpi.com
### DATE PREPARED:
1/4/2005
#### NAME OF MEDICAL DEVICE:
Classification Name: Catheter Introducer Common/Usual Name: General Percutaneous Introducer Needles Proprietary Name: AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles
## DEVICE CLASSIFICATION:
Classification Panel: General Hospital Class: II Procode: DYB Regulation Number: 21 CFR 870.1340
## STATEMENT OF SUBSTANTIAL EQUIVALENCE (Predicate Device References):
- 1. Safety Introducer Needles (K030135), B. Braun Medical, Inc., 901 Marcon Boulevard, Allentown, PA 18109.
- Majestik™ Angiographic Introducer Needles (pre-amendment), Merit Medical 2. Systems, Inc., 1600 West Merit Parkway South Jordan, Utah 84095.
## DEVICE DESCRIPTION:
The AdvancIntroducer™ needles consist of a stainless steel needle and a colored translucent standard female Luer lock hub locking connector for rapid (flashback) visualization. The hub has a bevel-up orientation indicator. The hub has been designed to provide the end-user excellent ergonomic tactile balance and stability. The AdvancIntroducer™ needles are available in one-wall with or without a Seldinger shield. The stainless steel needles are
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available with and without an echogenic feature or a specialty coating to enhance available war and with oneedles are available in a range of wall thicknesses, gauges and lengths to match the end-user need.
AdvancIntroducer™ needles will be marketed to the clinical end-user as sterile, nonpyrogenic, and single use devices. Additionally, the device will be marketed as the safety procedure needle in procedure trays. In the case of being used in procedural kits, the product will be shipped bulk non-sterile to the kitting manufacturer. The AdvancIntroducer™ will be incorporated into the procedure kit, packaged and sterilized.
SecureLoc™ Safety Introducer Needles have all the same components as the AdvancIntroducer™ and in addition, incorporates an intuitive easy to use safety guard which is an integral part of the device. SecureLoc™ Safety Introducer Needles are designed for common Introducer needle lengths and gauges. Obturators and stylettes are appropriately available. Stylette handles have an incorporated key to align to the cutting bevel.
The SecureLoc™ Safety Introducer Needle's safety engineered integral safety guard is advanced by the clinician. The safety guard automatically senses the end of the needle and locks a safety guard covering the needle tip. The SecureLoc™ Safety Introducer Needle's easy to use intuitive safety guard reduces the risk of accidental needlestick injuries by shielding the needle tip. A visual, tactile feel, and/or audible confirmation of the locking component over the needle confirms lockout of the safety guard over the needle. The sharps injury prevention guard cannot be deactivated and remains protective through disposal into a sharps container. The safety guard can be activated over stylettes, obturators, and guidewires.
SecureLoc™ Safety Introducer Needles will be marketed to the clinical end-user as sterile, non-pyrogenic, single use devices. Additionally, the device will be marketed as the safety procedure needle in procedure trays. In the case of being used in procedural kits, the product will be shipped bulk non-sterile to the kitting manufacturer. The SecureLoc™ Safety Introducer will be incorporated into the procedure kit, which is then packaged and sterilized.
## INTENDED USE:
Both the AdvancIntroducer™ and the SecureLoc™ Safety Introducer Needles are intended to be used for those patients requiring percutaneous procedures utilizing an introducer needle for guidewire placement for subsequent placement of catheters or other introducer needle required medical procedures.
The SecureLoc™ Safety Introducer Needle's safety engineered integral safety guard is advanced by the clinician. The safety guard automatically senses the end of the needle and locks covering the needle tip. The SecureLoc™ Safety Introducer Needle's easy to use intuitive safety guard reduces the risk of accidental needlestick injuries by shielding the needle point. The safety guard can be activated over stylettes, obturators, and guidewires.
The AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles will be marketed as both bulk non-sterile single use devices to procedural kit manufacturers and also as sterile, non-pyrogenic, single use devices to clinical end-users. The AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles may be used in any appropriate patient population. Page 15 of 72 Confidential
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# TECHNOLOGICAL COMPARISON TO PREDICATE DEVICES:
I is Specialized Health Products®, Inc.'s conclusion that the AdvancIntroducer™ and the It is Specialized Health Producer Needles are substantially equivalent to the following Secures: Safety Introducer Needles (K030135), B. Braun Medical, Inc., 901 Marcon acvices: Bajery Infroadco (1188) (1188) 118 Angiographic Introducer Needles (pre-Boutevard, Thentown, 11 1 10167 uns, Inc., 1600 West Merit Parkway South Jordan, Utah 84095
A summary of the key technological comparisons follows:
- The AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles are similar in . r the havane firstion, materials and use as the predicate Merit Medical Introducer needle devices.
- The SecureLoc™ Safety Introducer Needles have a safety guard that locks a safety . guard over the needle tip after the needle is removed from the patient, as does the B. Braun predicate device.
- The SecureLoc™ Safety Introducer Needle's safety guard lock-out can be confirmed . by visual means, tactile feel and/or audible means, as does the B. Braun predicate device cited in this submission.
## SUMMARY OF PERFORMANCE TESTING:
Comparative testing has been performed on the AdvancIntroducer™ and the SecureLoc™ Safety Introducer Needles and the predicate devices. Test results indicate that the AdvancIntroducer™ and SecureLoc™ Safety Introducer Needles perform in a substantially equivalent manner.
## SUMMARY OF SIMULATED USE STUDY:
A total of 500 SecureLoc™ Safety Introducer Needles were successfully inserted by clinicians into simulated tissue and activated. No sharps injuries or failures of the integral needlestick prevention guard/safety guard occurred.
## CONCLUSION:
The material testing and simulated use data demonstrate that the AdvancIntroducer™ and the SecureLoc™ Safety Introducer Needle are safe and effective for their intended use, comply with medical device standards, and are substantially equivalent to:
- Safety Introducer Needles (K030135), B. Braun Medical, Inc., 901 Marcon Boulevard, . Allentown, PA 18109.
- Majestik™ Angiographic Introducer Needles (pre-amendment), Merit Medical Systems, . Inc., 1600 West Merit Parkway South Jordan, Utah 84095.
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Image /page/3/Picture/1 description: The image is a black and white seal for the Department of Health & Human Services - USA. The seal is circular with the text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" arranged around the top half of the circle. Inside the circle is a stylized symbol that appears to be three overlapping human figures.
Public Health Service
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
FEB 1 8 2005
Mr. Mark Nelson Director, Quality and Regulatory Affairs Specialized Health Products® Incorporated 585 West 500 South #200 Bountiful, Utah 84010
Re: K050023
Trade/Device Name: AdvancIntroducer™ Introducer Needles and SecureLoc™ Safety Introducer Needles Regulation Number: 870.1340 Regulation Name: Catheter Introducer Regulatory Class: II Product Code: DYB Dated: January 3, 2005 Received: January 6, 2005
Dear Mr. Nelson:
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 mendments, 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 approvisions 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.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to such additional controls. Existing major regulations affecting (1 Wr.), it may be backed to the Code of Federal Regulations, Title 21, Parts 800 to 898. In your device ear. be foundsh further announcements concerning your device in the Federal Register.
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## Page 2 - Mr. Nelson
Please be advised that FDA's issuance of a substantial equivalence determination does not Please be advised that 1 DTC 3 lostained on that your device complies with other requirements mean that IDA has made a deceminations administered by other Federal agencies. of the Act of ally rederal states and registered to registerial woulding, but not limited to: registration You must comply with an the Fee requirements) ; good manufacturing practice and ifsing (21 CFR 1 art 007), labolity systems (QS) regulation (21 CFR Part 820); and if requirements as set form in the quality bysteins (Sections 531-542 of the Act); 21 CFR 1000-1050.
This letter will allow you to begin marketing your device as described in your Section 510(k) This letter will anow you to ocgan mading of substantial equivalence of your device to a premarket notification. The PDF miling of basesiation for your device and thus, permits your device to proceed to the market.
If you desire specific advice for your device on our labeling regulation (21 CFR Part 801), If you desire specific advice to: Jour de at (240) 276-0115. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the may obtain of Small Manufacturers, International and Consumer Assistance at its toll-free Division of 01618-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html.
Sincerely yours,
Chiu Lin, Ph.D.
Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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# INDICATIONS FOR USE STATEMENT
510(k) Number (if known): ____________________________________________________________________________________________________________________________________________________
Device Name: SecureLocTM Safety Introducer Needles
Indications for Use:
- SecureLoc™ Safety Introducer Needles are intended to be used for those patients . SecureDoc - Burety marcedures utilizing an introducer needle for guidewire requiring persualleous it placement of catheters or other introducer needle required medical procedures.
- The SecureLoc™ Safety Introducer Needles are intended to be used as integral . I he Secureboo - Baroy thase patients requiring percutaneous procedures utilizing an introducer needle for guidewire placement for subsequent placement of catheters or other introducer needle required medical procedures.
- or other matten Safety Introducer Needle's safety engineered integral safety guard . is advanced by the clinician. The safety guard automatically senses the end of the 15 advanced of the risk of accidental needlestick injuries by locking a safety necode and readed tip. The safety guard can be activated over stylettes, obturators, and guidewires.
- Will be marketed as bulk non-sterile single use devices to procedural kit . will be manifecturers and also as sterile, non-pyrogenic, single use devices to clinical endusers.
- May be used in any appropriate patient population. .
Prescription Use X (Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 807 Subpart C)
# (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
# Concurrence of CDRH, Office of Device Evaluation (ODE)
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# INDICATIONS FOR USE STATEMENT
510(k) Number (if known): ____________________________________________________________________________________________________________________________________________________
Device Name: AdvancIntroducer™ Introducer Needles
Indications for Use:
- AdvancIntroducer™ Introducer Needles are intended to be used with those patients . requiring percutaneous entry procedures utilizing an introducer needle for guidewire placement for subsequent placement of catheters or other introducer needle required medical procedures.
- Will be marketed as bulk non-sterile single use devices to procedural kit . manufacturers and also as sterile, non-pyrogenic, single use devices to clinical endusers.
- May be used in any appropriate patient population. .
Teresa Perez Ott
sion Sich-Off) island City-Office Infogy, General Hospital, noution Control, Dental Devices
10:50 Number:__ 154544 27
X Prescription Use (Part 21 CFR 801 Subpart D)
AND/OR
Over-The-Counter Use (21 CFR 807 Subpart C)
## (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
