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FDA 510(k)

MODIFIED AML + ACETABULAR CUP PROSTHESIS

K-Number: K900891 · 1990-03-12

ApplicantDepuy, Inc.
Decision Date1990-03-12
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

MODIFIED AML + ACETABULAR CUP 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 1990-03-12 under 510(k) number K900891. 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 MODIFIED AML + ACETABULAR CUP PROSTHESIS?

MODIFIED AML + ACETABULAR CUP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1990-03-12. The listed applicant is Depuy, Inc.. The 510(k) number is K900891.

When did MODIFIED AML + ACETABULAR CUP PROSTHESIS receive FDA 510(k) clearance?

MODIFIED AML + ACETABULAR CUP PROSTHESIS received FDA 510(k) clearance on 1990-03-12, under 510(k) number K900891.

Who is the listed applicant for MODIFIED AML + ACETABULAR CUP 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 MODIFIED AML + ACETABULAR CUP PROSTHESIS?

The FDA product code for MODIFIED AML + ACETABULAR CUP PROSTHESIS is JDI.

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Other records listing Depuy, Inc. as applicant

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Related Devices (Code: JDI)

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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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