FDA 510(k), CONDUIT Cages; FIBERGRAFT BG Putty, MCRA LLC

FDA 510(k), CONDUIT Cages; FIBERGRAFT BG Putty, MCRA LLC

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510(K) Number: K222276
Device Name: CONDUIT Cages; FIBERGRAFT BG Putty
Manufacturer: MCRA LLC
Device Classification Name: Intervertebral Fusion Device With Bone Graft, Cervical
Regulation Number: 888.3080
Classification Product Code: ODP
Date Received: 07/29/2022
Decision Date: 10/15/2022
Regulation Medical Specialty: Orthopedic
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