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FDA 510(k)

EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY

K-Number: K932690 · 1995-02-09

ApplicantExactech, Inc.
Decision Date1995-02-09
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY is the device name listed in this FDA 510(k) record. The listed applicant is Exactech, Inc.. It received FDA 510(k) clearance on 1995-02-09 under 510(k) number K932690. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY?

EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY is a medical device that received FDA 510(k) clearance on 1995-02-09. The listed applicant is Exactech, Inc.. The 510(k) number is K932690.

When did EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY receive FDA 510(k) clearance?

EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY received FDA 510(k) clearance on 1995-02-09, under 510(k) number K932690.

Who is the listed applicant for EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY?

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

What is the FDA product code for EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY?

The FDA product code for EXACTECH CRUCIATE RETAINING CEMENTED TOTAL KNEE SY is JWH.

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Related Devices (Code: JWH)

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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