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FDA 510(k)

STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM

K-Number: K032901 · 2003-12-02

ApplicantStryker Endoscopy
Decision Date2003-12-02
Product CodeGAT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Endoscopy. It received FDA 510(k) clearance on 2003-12-02 under 510(k) number K032901. 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 STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM?

STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM is a medical device that received FDA 510(k) clearance on 2003-12-02. The listed applicant is Stryker Endoscopy. The 510(k) number is K032901.

When did STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM receive FDA 510(k) clearance?

STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM received FDA 510(k) clearance on 2003-12-02, under 510(k) number K032901.

Who is the listed applicant for STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM?

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

What is the FDA product code for STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM?

The FDA product code for STRYKER MINI-MENDER MENISCAL REPAIR SYSTEM is GAT.

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Related Devices (Code: GAT)

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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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