FDA device listing
IdentiTi ALIF Standalone Interbody System,IdentiTi NanoTec ALIF Standalone Interbody System,IdentiTi NanoTec Interbody…
FDA device listing 1730566642 · ALPHATEC HOLDINGS, INC.
Key facts
| Proprietary names | IdentiTi ALIF Standalone Interbody System,IdentiTi NanoTec ALIF Standalone Interbody System,IdentiTi NanoTec Interbody System,IdentiTi Porous Ti Interbody System,Transcend NanoTec Interbody System,Transcend PEEK Interbody System |
|---|---|
| Owner/operator | ALPHATEC HOLDINGS, INC. |
| Owner/operator number | 9072657 |
| Premarket submissions | K222028 |
| Product codes | MAX, OVD, PHM |
| Device names | MAX - Intervertebral Fusion Device With Bone Graft, Lumbar, OVD - Intervertebral Fusion Device With Integrated Fixation, Lumbar, PHM - Intervertebral Fusion Device With Bone Graft, Thoracic |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3080 |
| Review panels | Orthopedic |
| Registered establishments | Alphatec Spine, Inc., ALPHATEC SPINE, INC. |
| Establishment registrations | 2027467, 3019878714 |
| FEI numbers | 2027467, 3019878714 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1,000+ UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database