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FDA 510(k)

CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE

K-Number: K102339 · 2010-11-23

ApplicantConmed Linvatec
Decision Date2010-11-23
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Conmed Linvatec. It received FDA 510(k) clearance on 2010-11-23 under 510(k) number K102339. The device is classified under product code GAT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE?

CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE is a medical device that received FDA 510(k) clearance on 2010-11-23. The listed applicant is Conmed Linvatec. The 510(k) number is K102339.

When did CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE receive FDA 510(k) clearance?

CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE received FDA 510(k) clearance on 2010-11-23, under 510(k) number K102339.

Who is the listed applicant for CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE?

The FDA 510(k) record lists Conmed Linvatec as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE?

The FDA product code for CONMED LINVATEC SEQUENT MENISCAL REPAIR DEVICE is GAT.

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Other records listing Conmed Linvatec as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K111779Y-KNOT ALL-SUTURE ANCHOR MODEL HF13K102410MATRYX INTERFERENCE SCREW (5.0-6.5MM)K101100CROSSFT OC SUTURE ANCHOR MODE CFC-4502, CFC-5502, CFC-6502, CFC-4503, CFC-5503, CFC-6503K092898CONMED LINVATEC PRESTO PRELOADED WITH ONE OR TWO #2 HI-FI SUTURESK090560CONMED LINVATEC ANODIZED ALUMINUM STERILIZATION TRAYSK083161ZEN WIRELESS FOOTSWITCH (W1000), ZEN WIRELESS FOOTSWITCH ADAPTER (W1100)

View all 21 devices →

Related Devices (Code: GAT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253910Stitch - Suture Wires and TapesGM Dos Reis Industria e Comercio Ltda.K261021EasyWhip FamilyWinter Innovations, Inc.K260775Polyethylene;Polyethylene Fusion;Polyethylene OrthoTape™Teleflex Medical, LLCK254275HyperSuture All Green Extension LineThreadstone, LLCK254188Meniscus VersaflexGM Dos Reis Industria e Comercio Ltda.K253145Pre-Sutured TendonRti Surgical, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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