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FDA 510(k)

PROSTHETIC CEMENT REMOVER

K-Number: K890285 · 1989-04-19

ApplicantAlbert K. Chin
Decision Date1989-04-19
Product CodeLZV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PROSTHETIC CEMENT REMOVER is the device name listed in this FDA 510(k) record. The listed applicant is Albert K. Chin. It received FDA 510(k) clearance on 1989-04-19 under 510(k) number K890285. The device is classified under product code LZV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROSTHETIC CEMENT REMOVER?

PROSTHETIC CEMENT REMOVER is a medical device that received FDA 510(k) clearance on 1989-04-19. The listed applicant is Albert K. Chin. The 510(k) number is K890285.

When did PROSTHETIC CEMENT REMOVER receive FDA 510(k) clearance?

PROSTHETIC CEMENT REMOVER received FDA 510(k) clearance on 1989-04-19, under 510(k) number K890285.

Who is the listed applicant for PROSTHETIC CEMENT REMOVER?

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

What is the FDA product code for PROSTHETIC CEMENT REMOVER?

The FDA product code for PROSTHETIC CEMENT REMOVER is LZV.

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Related Devices (Code: LZV)

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.

K021502OSCAR, MODEL OE3000Orthosonics, Ltd.K961101STRYKER CEMENT REMOVAL SYSTEMStryker Corp.K930629ACRYL-X II SYSTEMSonokinetics, Inc.K904156ORIGIN(TM) CEMENT EXTRACT SYST STD-PR/SPL-PR KITSOrigin Medsystems, Inc.K904180PROSTHETIC CEMENT REMOVEROrigin Medsystems, Inc.K891472IMPLANT TECHNOLOGY BONE CEMENT EXTRACTORImplant Technology, Inc.

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.

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