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Intervertebral Fusion Device With Bone Graft, Thoracic

FDA product code PHM · Class 2 · Orthopedic

22,477

Registered devices

23

Adverse events

0

Recalls

3

510(k) clearances

Devices with this code

HEDRON — GLOBUS MEDICAL, INC.CoRoent — Nuvasive, Inc.CoRoent — Nuvasive, Inc.IDENTITI — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.IDENTITi NANOTEC — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.TRANSCEND NANOTEC — ALPHATEC SPINE, INC.TRANSCEND NANOTEC — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.IdentiTi II — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.Solar™ Interbody Fusion System — DEGEN MEDICAL, INC.Solar™ Interbody Fusion System — DEGEN MEDICAL, INC.Solar™ Interbody Fusion System — DEGEN MEDICAL, INC.Solar™ Interbody Fusion System — DEGEN MEDICAL, INC.CoRoent — Nuvasive, Inc.TLX — Nuvasive, Inc.Battalion — ALPHATEC SPINE, INC.IDENTITI — ALPHATEC SPINE, INC.IdentiTi — ALPHATEC SPINE, INC.IDENTITi NANOTEC — ALPHATEC SPINE, INC.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.