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FDA 510(k)

CLOUTIER II TOTAL KNEE W/BEADED SURF

K-Number: K841517 · 1984-08-30

ApplicantZimmer, Inc.
Decision Date1984-08-30
Product Code
DecisionSubstantially Equivalent

Device Summary

CLOUTIER II TOTAL KNEE W/BEADED SURF is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1984-08-30 under 510(k) number K841517. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLOUTIER II TOTAL KNEE W/BEADED SURF?

CLOUTIER II TOTAL KNEE W/BEADED SURF is a medical device that received FDA 510(k) clearance on 1984-08-30. The listed applicant is Zimmer, Inc.. The 510(k) number is K841517.

When did CLOUTIER II TOTAL KNEE W/BEADED SURF receive FDA 510(k) clearance?

CLOUTIER II TOTAL KNEE W/BEADED SURF received FDA 510(k) clearance on 1984-08-30, under 510(k) number K841517.

Who is the listed applicant for CLOUTIER II TOTAL KNEE W/BEADED SURF?

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

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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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