FDA 510(k)

DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500)

K-Number: K962923 · 1996-10-01

Decision Date1996-10-01

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500) is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1996-10-01 under 510(k) number K962923. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500)?

DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500) is a medical device that received FDA 510(k) clearance on 1996-10-01. The listed applicant is Depuy, Inc.. The 510(k) number is K962923.

When did DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500) receive FDA 510(k) clearance?

DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500) received FDA 510(k) clearance on 1996-10-01, under 510(k) number K962923.

Who is the listed applicant for DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500)?

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 GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500)?

The FDA product code for DEPUY GRADED POROSITY AML HIP (1371-03/06-500/1371-43/46-500) is LPH.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.