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FDA 510(k)

ACETABULAR CEMENT COMPRESSOR

K-Number: K803165 · 1980-12-31

ApplicantZimmer, Inc.
Decision Date1980-12-31
Product CodeHXO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACETABULAR CEMENT COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1980-12-31 under 510(k) number K803165. The device is classified under product code HXO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETABULAR CEMENT COMPRESSOR?

ACETABULAR CEMENT COMPRESSOR is a medical device that received FDA 510(k) clearance on 1980-12-31. The listed applicant is Zimmer, Inc.. The 510(k) number is K803165.

When did ACETABULAR CEMENT COMPRESSOR receive FDA 510(k) clearance?

ACETABULAR CEMENT COMPRESSOR received FDA 510(k) clearance on 1980-12-31, under 510(k) number K803165.

Who is the listed applicant for ACETABULAR CEMENT COMPRESSOR?

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 ACETABULAR CEMENT COMPRESSOR?

The FDA product code for ACETABULAR CEMENT COMPRESSOR is HXO.

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Related Devices (Code: HXO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K885305ACETABULAR CUP PUSHER/IMPACTORCobot Medical Corp.K771072INSERTEO, META.-PHAL.&THUMB CARPO-METADepuy, Inc.

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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