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FDA 510(k)

POROCOAT TM TOWNLEY ANATOMIC KNEE

K-Number: K810326 · 1981-03-11

ApplicantDepuy, Inc.
Decision Date1981-03-11
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POROCOAT TM TOWNLEY ANATOMIC KNEE is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1981-03-11 under 510(k) number K810326. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POROCOAT TM TOWNLEY ANATOMIC KNEE?

POROCOAT TM TOWNLEY ANATOMIC KNEE is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is Depuy, Inc.. The 510(k) number is K810326.

When did POROCOAT TM TOWNLEY ANATOMIC KNEE receive FDA 510(k) clearance?

POROCOAT TM TOWNLEY ANATOMIC KNEE received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810326.

Who is the listed applicant for POROCOAT TM TOWNLEY ANATOMIC KNEE?

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

What is the FDA product code for POROCOAT TM TOWNLEY ANATOMIC KNEE?

The FDA product code for POROCOAT TM TOWNLEY ANATOMIC KNEE 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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