FDA 510(k)

SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL

Numéro K : K161710 · 2017-06-29

DemandeurSpinal Analytics & Geometrical Impant Co, LLC

Date de décision2017-06-29

Code produitMAX

Comité consultatifOR

DécisionSubstantially Equivalent

Résumé du dispositif

SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL is the device name listed in this FDA 510(k) record. The listed applicant is Spinal Analytics & Geometrical Impant Co, LLC. It received FDA 510(k) clearance on 2017-06-29 under 510(k) number K161710. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL?

SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL is a medical device that received FDA 510(k) clearance on 2017-06-29. The listed applicant is Spinal Analytics & Geometrical Impant Co, LLC. The 510(k) number is K161710.

When did SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL receive FDA 510(k) clearance?

SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL received FDA 510(k) clearance on 2017-06-29, under 510(k) number K161710.

Who is the listed applicant for SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL?

The FDA 510(k) record lists Spinal Analytics & Geometrical Impant Co, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL?

The FDA product code for SAGICO IBF SYSTEM – ARIA LUMBAR, SAGICO IBF SYSTEM – ARION CERVICAL is MAX.

Essais cliniques associés

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Dispositifs connexes (Code : MAX)

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Source officielle

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