FDA 510(k)

IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS

K-Number: K932923 · 1994-05-03

Decision Date1994-05-03

Product CodeLPH

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS is the device name listed in this FDA 510(k) record. The listed applicant is Implex Corp.. It received FDA 510(k) clearance on 1994-05-03 under 510(k) number K932923. 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 IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS?

IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS is a medical device that received FDA 510(k) clearance on 1994-05-03. The listed applicant is Implex Corp.. The 510(k) number is K932923.

When did IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS receive FDA 510(k) clearance?

IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS received FDA 510(k) clearance on 1994-05-03, under 510(k) number K932923.

Who is the listed applicant for IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS?

The FDA 510(k) record lists Implex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS?

The FDA product code for IMPLEX A-230 POROUS ACETABULAR CUP SYST.CEMENTLESS is LPH.

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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.