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FDA 510(k)

DEPUY HIP PROSTHESIS

K-Number: K914078 · 1993-01-07

ApplicantDepuy, Inc.
Decision Date1993-01-07
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DEPUY HIP 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 1993-01-07 under 510(k) number K914078. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY HIP PROSTHESIS?

DEPUY HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1993-01-07. The listed applicant is Depuy, Inc.. The 510(k) number is K914078.

When did DEPUY HIP PROSTHESIS receive FDA 510(k) clearance?

DEPUY HIP PROSTHESIS received FDA 510(k) clearance on 1993-01-07, under 510(k) number K914078.

Who is the listed applicant for DEPUY HIP 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 DEPUY HIP PROSTHESIS?

The FDA product code for DEPUY HIP PROSTHESIS is JDI.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: JDI)

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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