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FDA 510(k)

LCS FEMORAL HIP PROSTHESIS

K-Number: K880269 · 1988-05-06

ApplicantDepuy, Inc.
Decision Date1988-05-06
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

LCS FEMORAL 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 1988-05-06 under 510(k) number K880269. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the LCS FEMORAL HIP PROSTHESIS?

LCS FEMORAL HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1988-05-06. The listed applicant is Depuy, Inc.. The 510(k) number is K880269.

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

LCS FEMORAL HIP PROSTHESIS received FDA 510(k) clearance on 1988-05-06, under 510(k) number K880269.

Who is the listed applicant for LCS FEMORAL 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 LCS FEMORAL HIP PROSTHESIS?

The FDA product code for LCS FEMORAL 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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