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FDA 510(k)

ARTHROSCOPY SYSTEM LEG HOLDER

K-Number: K821029 · 1982-04-29

ApplicantZimmer, Inc.
Decision Date1982-04-29
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPY SYSTEM LEG HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1982-04-29 under 510(k) number K821029. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPY SYSTEM LEG HOLDER?

ARTHROSCOPY SYSTEM LEG HOLDER is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is Zimmer, Inc.. The 510(k) number is K821029.

When did ARTHROSCOPY SYSTEM LEG HOLDER receive FDA 510(k) clearance?

ARTHROSCOPY SYSTEM LEG HOLDER received FDA 510(k) clearance on 1982-04-29, under 510(k) number K821029.

Who is the listed applicant for ARTHROSCOPY SYSTEM LEG HOLDER?

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

What is the FDA product code for ARTHROSCOPY SYSTEM LEG HOLDER?

The FDA product code for ARTHROSCOPY SYSTEM LEG HOLDER is FWZ.

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Related Devices (Code: FWZ)

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.

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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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