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FDA 510(k)

IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR

K-Number: K891472 · 1989-05-02

ApplicantImplant Technology, Inc.
Decision Date1989-05-02
Product CodeLZV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR is the device name listed in this FDA 510(k) record. The listed applicant is Implant Technology, Inc.. It received FDA 510(k) clearance on 1989-05-02 under 510(k) number K891472. 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 IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR?

IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR is a medical device that received FDA 510(k) clearance on 1989-05-02. The listed applicant is Implant Technology, Inc.. The 510(k) number is K891472.

When did IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR receive FDA 510(k) clearance?

IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR received FDA 510(k) clearance on 1989-05-02, under 510(k) number K891472.

Who is the listed applicant for IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR?

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

What is the FDA product code for IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR?

The FDA product code for IMPLANT TECHNOLOGY BONE CEMENT EXTRACTOR is LZV.

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Other records listing Implant Technology, Inc. as applicant

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.

K921525HIP JOINT METAL/POLYMER SEMI-CONSTRAINED PROTHESISK915617LSF HA COATED FEMORAL HIPK920021LSF TOTAL HIP SYSTEM - MULLER-TYPE ACETABULAR CUPK913616LSF DIAGNOSTIC RELATED GROUP CEMENTED HIPK902727LSF CEMENTED FEMORAL HIPK901460LSF(TM) TOTAL HIP SYSTEM

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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.K890285PROSTHETIC CEMENT REMOVERAlbert K. Chin

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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