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FDA 510(k), K161642, CAVUX™ Cervical Cage
FDA 510(k), K161642, CAVUX™ Cervical Cage
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510(K) Number: K161642
Device Name: CAVUX™ Cervical Cage
Manufacturer: Margaret Wong
Device Classification Name: Intervertebral Fusion Device With Bone Graft, Cervical
Regulation Number: ODP
Classification Product Code: 06/14/2016
Date Received: 10/07/2016
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
Device Name: CAVUX™ Cervical Cage
Manufacturer: Margaret Wong
Device Classification Name: Intervertebral Fusion Device With Bone Graft, Cervical
Regulation Number: ODP
Classification Product Code: 06/14/2016
Date Received: 10/07/2016
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Orthopedic
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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