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FDA 510(k)

MENISCAL CINCH

K-Number: K073149 · 2008-02-11

ApplicantArthrex, Inc.
Decision Date2008-02-11
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MENISCAL CINCH is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2008-02-11 under 510(k) number K073149. 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 MENISCAL CINCH?

MENISCAL CINCH is a medical device that received FDA 510(k) clearance on 2008-02-11. The listed applicant is Arthrex, Inc.. The 510(k) number is K073149.

When did MENISCAL CINCH receive FDA 510(k) clearance?

MENISCAL CINCH received FDA 510(k) clearance on 2008-02-11, under 510(k) number K073149.

Who is the listed applicant for MENISCAL CINCH?

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

What is the FDA product code for MENISCAL CINCH?

The FDA product code for MENISCAL CINCH is GAT.

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Other records listing Arthrex, Inc. as applicant

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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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