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FDA 510(k)

GENERATION 5 LINKOW BLADE IMPLANTS

K-Number: K822969 · 1982-11-04

ApplicantLeonard P. Linkow, D.D.L.
Decision Date1982-11-04
Product CodeNRQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GENERATION 5 LINKOW BLADE IMPLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Leonard P. Linkow, D.D.L.. It received FDA 510(k) clearance on 1982-11-04 under 510(k) number K822969. The device is classified under product code NRQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERATION 5 LINKOW BLADE IMPLANTS?

GENERATION 5 LINKOW BLADE IMPLANTS is a medical device that received FDA 510(k) clearance on 1982-11-04. The listed applicant is Leonard P. Linkow, D.D.L.. The 510(k) number is K822969.

When did GENERATION 5 LINKOW BLADE IMPLANTS receive FDA 510(k) clearance?

GENERATION 5 LINKOW BLADE IMPLANTS received FDA 510(k) clearance on 1982-11-04, under 510(k) number K822969.

Who is the listed applicant for GENERATION 5 LINKOW BLADE IMPLANTS?

The FDA 510(k) record lists Leonard P. Linkow, D.D.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENERATION 5 LINKOW BLADE IMPLANTS?

The FDA product code for GENERATION 5 LINKOW BLADE IMPLANTS is NRQ.

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Related Devices (Code: NRQ)

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.

K211872PiezoImplant SystemRex Implants, Inc.K981954VARIOUS DENTAL IMPLANTS WITH VARIOUS ABUTMENTSHealthline Implants, Inc.K791366ORATRONICS ENDOSSEOUS FRAME ASSEMBLYOratronics, Inc.K791204MITER ENDOSTEAL BLADE IMPLANTDepuy, 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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