FDA 510(k)

BRIDALVEIL Occipital Cervical Thoracic System

Número K: K171250 · 2017-10-02

Data da decisão2017-10-02

Código do produtoNKG

Comité consultivoOR

DecisãoSubstantially Equivalent

Resumo do dispositivo

BRIDALVEIL Occipital Cervical Thoracic System is the device name listed in this FDA 510(k) record. The listed applicant is Astura Medical. It received FDA 510(k) clearance on 2017-10-02 under 510(k) number K171250. The device is classified under product code NKG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the BRIDALVEIL Occipital Cervical Thoracic System?

BRIDALVEIL Occipital Cervical Thoracic System is a medical device that received FDA 510(k) clearance on 2017-10-02. The listed applicant is Astura Medical. The 510(k) number is K171250.

When did BRIDALVEIL Occipital Cervical Thoracic System receive FDA 510(k) clearance?

BRIDALVEIL Occipital Cervical Thoracic System received FDA 510(k) clearance on 2017-10-02, under 510(k) number K171250.

Who is the listed applicant for BRIDALVEIL Occipital Cervical Thoracic System?

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

What is the FDA product code for BRIDALVEIL Occipital Cervical Thoracic System?

The FDA product code for BRIDALVEIL Occipital Cervical Thoracic System is NKG.

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Fonte oficial

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