← Product Code [HRX](/submissions/OR/subpart-b%E2%80%94diagnostic-devices/HRX) · K131191 # 4MM & 5MM FULL RADIUS BLADE PLUS, 4MM & 5MM BARREL BUR PLUS/4MM BARREL TORNADO BUR PLUS, 4MM & 5MM AGGRESSIVE BLADE PLUS (K131191) _Depuy Mitek, A Johnson & Johnson Company · HRX · Jul 22, 2013 · Orthopedic · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-b%E2%80%94diagnostic-devices/HRX/K131191 ## Device Facts - **Applicant:** Depuy Mitek, A Johnson & Johnson Company - **Product Code:** [HRX](/submissions/OR/subpart-b%E2%80%94diagnostic-devices/HRX.md) - **Decision Date:** Jul 22, 2013 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 888.1100 - **Device Class:** Class 2 - **Review Panel:** Orthopedic - **Attributes:** Therapeutic ## Indications for Use The FMS Blades and Burrs are an accessory to the FMS Fluid Management Systems. FMS Blades and Burrs are intended to provide controlled cutting, burring, shaving and abrading of bone and tissue for use in arthroscopic surgery. ## Device Story FMS Shaver Blades and Burrs function as accessories to FMS Fluid Management System handpieces (Tornado or Micro). Device consists of stainless steel outer tube and rotating inner tube with plastic hubs; distal tips feature sharp edges for mechanical cutting. Operated by surgeons during arthroscopic procedures to remove or shape bone and tissue. Performance modifications include updated materials, adjusted blade window profiles, and altered burr tip geometry to enhance cutting efficiency. Device provides mechanical cutting action; no electronic or software components involved. ## Clinical Evidence Bench testing only. Verification activities included blade tissue cutting, burr bone cutting, and blade/burr shed testing. Results demonstrated performance and safety equivalent to predicate devices. ## Technological Characteristics Stainless steel tubes; plastic hubs. Mechanical cutting/abrading principle. Dimensions/geometry modified for performance. No energy source, connectivity, or software. Sterilization method not specified. ## Regulatory Identification An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint. ## Predicate Devices - FMS DUO pump and shaver system ([K954465](/device/K954465.md)) - NeXtraTM arthroscopic pump and shaver system ([K041824](/device/K041824.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0}------------------------------------------------ | | K131191 | | JUL 22 | |---------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------|--------| | 510(k) SUMMARY | | | | | Submitter's Name and
Address | Susan Kagan
Project Manager, Regulatory Affairs
DePuy Mitek, Inc.
a Johnson & Johnson company
325 Paramount Drive
Raynham, MA 02767 | Telephone: 508-880-8097
Facsimile: 508-977-6911
e-mail: skagan@its.jnj.com | | | | Date Prepared: April 25, 2013 | | | | Name of Medical Device | Proprietary Name:
Common Name: | FMS Shaver Blades and Burrs
Blades and Burrs | | | Substantial Equivalence | Blades and Burrs for FMS Fluid Management System Shavers are
substantially equivalent to the Blades and Burrs covered in the following
cleared systems:
• K954465 - FMS DUO pump and shaver system
• K041824 - NeXtraTM arthroscopic pump and shaver system | | | | Device Classification | Classification Name:
Arthroscope
Classification Number:
21 CFR 888.1100 Class II
Product Code:
HRX | | | | Device Description | The purpose of this 510(k) Notification is to outline modifications made to
the currently marketed FMS Blades and Burrs. The changes being made to
the proposed devices are to enhance performance and include modifications
including: material changes, modified inner and outer blade window profiles,
and modified inner and outer burr tip geometry. | | | | | FMS Shaver Blades and Burrs are used with the FMSTM Tornado or Micro
Hand pieces which are accessories to the and Fluid Management Systems.
They consist of stainless steel outer tube and a rotating inner tube connected
to an inner and outer plastic hubs. Distal tips of the tubes contain sharp edges
to facilitate the cutting. | | | | Indications for Use | The FMS Blades and Burrs are an accessory to the FMS Fluid Management
Systems. FMS Blades and Burrs are intended to provide controlled cutting,
burring, shaving and abrading of bone and tissue for use in arthroscopic | | | FMS Blades and Burrs Traditional 510(k) · {1}------------------------------------------------ K131191 surgery. | Nonclinical Testing | Verification activities such as Blade Tissue Cutting, Burr Bone Cutting, Blade Shed Testing and Burr Shed Testing were performed on the proposed and predicate devices. | |------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------| | Safety and Performance | Results of performance and safety testing have demonstrated that the modified devices are substantially equivalent to the predicate devices. | | | Based on the indications for use, technological characteristics, and comparison to predicate devices, the proposed Blades and Burrs have been shown to be substantially equivalent to predicate devices under the Federal Food, Drug and Cosmetic Act. | FMS Blades and Burrs Traditional 510(k) · · : {2}------------------------------------------------ Image /page/2/Picture/0 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo consists of a stylized eagle with its wings spread, and the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" are arranged in a circular pattern around the eagle. The eagle is black, and the text is also black. The logo is simple and recognizable. ## DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 10903 New Hampshire Avenue Document Control Center - WO66-G609 Silver Spring, MD 20993-0002 DePuy Mitek Incorporated a Johnson & Johnson Company % Ms. Susan Kagan Project Manager, Regulatory Affairs 325 Paramount Drive Raynham. Massachusetts 02767 ymann, IVR33 Re: K131191 Trade/Device Name: Blades and Burrs for FMS Shavers Regulation Number: 21 CFR 888.1100 Regulation Name: Arthroscope Regulatory Class: Class II Product Codc: HRX Dated: April 25, 2013 Received: April 26, 2013 Dear Ms. Kagan: 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 docs not evaluate information related to contract liability warranties. We remind you; however, that device labeling must be truthful and not mislcading. 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); medical device reporting (reporting of medical device-related adverse events) (21 CFR 803); good manufacturing practice requirements as set July 22, 2013 {3}------------------------------------------------ ## Page 2 - Ms. Susan Kagan 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), please contact the Division of Small Manufacturers, International and Consumer Assistance at its tollfree 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" (21CFR 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 Small Manufacturers, International and Consumer Assistance 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, Mark N. Melkerson -S Mark N. Melkerson Acting Director Division of Surgical Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ ## INDICATION FOR USE STATEMENT ## INDICATIONS FOR USE 510(k) Number (if known): K131191 Device Name: Blades and Burrs for FMS Shavers Indications for Use: The FMS Blades and Burrs are an accessory to the FMS Fluid Management Systems. FMS Blades and Burrs are intended to provide controlled cutting, burring, shaving and abrading of bone and tissue for use in arthroscopic surgery. V 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) Page I of 1 **Joshua C. Nipper -S** (Division Sign-Off) Division of Surgical Devices 510(k) Number: K131191 --- **Source:** [https://fda.innolitics.com/submissions/OR/subpart-b%E2%80%94diagnostic-devices/HRX/K131191](https://fda.innolitics.com/submissions/OR/subpart-b%E2%80%94diagnostic-devices/HRX/K131191) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com