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FDA 510(k)

STABILITY FEMORAL PROSTHESIS W/HAP

K-Number: K915655 · 1994-02-14

ApplicantDepuy, Inc.
Decision Date1994-02-14
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

STABILITY FEMORAL PROSTHESIS W/HAP is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1994-02-14 under 510(k) number K915655. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STABILITY FEMORAL PROSTHESIS W/HAP?

STABILITY FEMORAL PROSTHESIS W/HAP is a medical device that received FDA 510(k) clearance on 1994-02-14. The listed applicant is Depuy, Inc.. The 510(k) number is K915655.

When did STABILITY FEMORAL PROSTHESIS W/HAP receive FDA 510(k) clearance?

STABILITY FEMORAL PROSTHESIS W/HAP received FDA 510(k) clearance on 1994-02-14, under 510(k) number K915655.

Who is the listed applicant for STABILITY FEMORAL PROSTHESIS W/HAP?

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 STABILITY FEMORAL PROSTHESIS W/HAP?

The FDA product code for STABILITY FEMORAL PROSTHESIS W/HAP is MEH.

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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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