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FDA 510(k)

SYNTHES CERVICAL VERTABRAE PLATES

K-Number: K792352 · 1979-12-06

ApplicantDePuy Synthes
Decision Date1979-12-06
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SYNTHES CERVICAL VERTABRAE PLATES is the device name listed in this FDA 510(k) record. The listed applicant is DePuy Synthes. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792352. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHES CERVICAL VERTABRAE PLATES?

SYNTHES CERVICAL VERTABRAE PLATES is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is DePuy Synthes. The 510(k) number is K792352.

When did SYNTHES CERVICAL VERTABRAE PLATES receive FDA 510(k) clearance?

SYNTHES CERVICAL VERTABRAE PLATES received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792352.

Who is the listed applicant for SYNTHES CERVICAL VERTABRAE PLATES?

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

What is the FDA product code for SYNTHES CERVICAL VERTABRAE PLATES?

The FDA product code for SYNTHES CERVICAL VERTABRAE PLATES is KWQ.

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Other records listing DePuy Synthes 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.

K233696DePuy Synthes Retrograde Femoral Nail Advanced SystemK233256Robotic Integration InstrumentsK233255CROSSNAV Navigation Enabled InstrumentsK233254TELIGEN System Navigation Ready InstrumentsK233665DePuy Synthes VOLT Mini Fragment Plating System, DePuy Synthes VOLT Small Fragment Plating SystemK231922DEPUY SYNTHES MAXFRAME AUTOSTRUT System

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Related Devices (Code: KWQ)

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.

K262149corra® cervical plating systemCarlsmed, Inc.K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLCK252776ARIES Anterior Cervical Plate SystemsZheJiang Decans Medical Devices Co., Ltd.K261112CastleLoc-P Anterior Cervical Plate SystemL&K BIOMED Co., Ltd.K260570corra™ cervical plating systemCarlsmed, Inc.K260697VyPlate™ Anterior Cervical Plate SystemVy Spine, LLC

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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