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FDA 510(k)

POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS

K-Number: K872025 · 1987-08-18

ApplicantDepuy, Inc.
Decision Date1987-08-18
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1987-08-18 under 510(k) number K872025. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS?

POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS is a medical device that received FDA 510(k) clearance on 1987-08-18. The listed applicant is Depuy, Inc.. The 510(k) number is K872025.

When did POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS receive FDA 510(k) clearance?

POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS received FDA 510(k) clearance on 1987-08-18, under 510(k) number K872025.

Who is the listed applicant for POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS?

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 (R) PROXIMAL FEMORAL THIRD PROSTHESIS?

The FDA product code for POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS is KWL.

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Related Devices (Code: KWL)

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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