FDA 510(k)

CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments

Numéro K : K223688 · 2023-03-08

Date de décision2023-03-08

Code produitMAX

Comité consultatifOR

DécisionSubstantially Equivalent

Résumé du dispositif

CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Medos International Sàrl. It received FDA 510(k) clearance on 2023-03-08 under 510(k) number K223688. 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 CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments?

CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments is a medical device that received FDA 510(k) clearance on 2023-03-08. The listed applicant is Medos International Sàrl. The 510(k) number is K223688.

When did CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments receive FDA 510(k) clearance?

CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments received FDA 510(k) clearance on 2023-03-08, under 510(k) number K223688.

Who is the listed applicant for CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments?

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

What is the FDA product code for CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments?

The FDA product code for CONDUIT™ Lateral Lumbar Intervertebral Fusion Cage, CONDUIT™ Instruments is MAX.

Essais cliniques associés

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Source officielle

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