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FDA 510(k)

ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32

K-Number: K030153 · 2003-04-01

ApplicantZimmer, Inc.
Decision Date2003-04-01
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32 is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2003-04-01 under 510(k) number K030153. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32?

ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32 is a medical device that received FDA 510(k) clearance on 2003-04-01. The listed applicant is Zimmer, Inc.. The 510(k) number is K030153.

When did ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32 receive FDA 510(k) clearance?

ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32 received FDA 510(k) clearance on 2003-04-01, under 510(k) number K030153.

Who is the listed applicant for ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32?

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

What is the FDA product code for ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32?

The FDA product code for ZCA ALL-POLY ACETABULAR CUP, SNAP-IN, MODEL 8005-946/958-32 is JDI.

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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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