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FDA 510(k)

MODIFIED PROFILE HIP ACETABULAR PROSTHESIS

K-Number: K891408 · 1989-06-12

ApplicantDepuy, Inc.
Decision Date1989-06-12
Product CodeJDX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFIED PROFILE HIP ACETABULAR 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 1989-06-12 under 510(k) number K891408. The device is classified under product code JDX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED PROFILE HIP ACETABULAR PROSTHESIS?

MODIFIED PROFILE HIP ACETABULAR PROSTHESIS is a medical device that received FDA 510(k) clearance on 1989-06-12. The listed applicant is Depuy, Inc.. The 510(k) number is K891408.

When did MODIFIED PROFILE HIP ACETABULAR PROSTHESIS receive FDA 510(k) clearance?

MODIFIED PROFILE HIP ACETABULAR PROSTHESIS received FDA 510(k) clearance on 1989-06-12, under 510(k) number K891408.

Who is the listed applicant for MODIFIED PROFILE HIP ACETABULAR 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 PROFILE HIP ACETABULAR PROSTHESIS?

The FDA product code for MODIFIED PROFILE HIP ACETABULAR PROSTHESIS is JDX.

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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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