FDA 510(k)

Vorderes Fersenspreizer zur Behandlung von Flexionskontrakturen nach Totaler Knieendoprothese

K-Nummer: K202972 · 2020-11-24

Entscheidungsdatum2020-11-24

ProduktcodeKWQ

BeratungsausschussOR

EntscheidungSubstantially Equivalent

Produktübersicht

Anterior Cervical Plate System is the device name listed in this FDA 510(k) record. The listed applicant is Nutech Spine and Biologics. It received FDA 510(k) clearance on 2020-11-24 under 510(k) number K202972. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Häufig gestellte Fragen

What is the Anterior Cervical Plate System?

Anterior Cervical Plate System is a medical device that received FDA 510(k) clearance on 2020-11-24. The listed applicant is Nutech Spine and Biologics. The 510(k) number is K202972.

When did Anterior Cervical Plate System receive FDA 510(k) clearance?

Anterior Cervical Plate System received FDA 510(k) clearance on 2020-11-24, under 510(k) number K202972.

Who is the listed applicant for Anterior Cervical Plate System?

The FDA 510(k) record lists Nutech Spine and Biologics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Anterior Cervical Plate System?

The FDA product code for Anterior Cervical Plate System is KWQ.

Zugehörige klinische Studien

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Verwandte Geräte (Code: KWQ)

K262149corra® cervical plating systemCarlsmed, Inc.K261309Palisades™ Buttress Plate SystemBethesda Medical Devices, LLC K252776ARIES Vorderes Halsplatten-SystemZheJiang 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

Offizielle Quelle

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