The following data is part of a premarket notification filed by Alphatec Spine with the FDA for Identiti™ Porous Ti Interbody System, Identiti™ Nanotec™ Interbody System, Transcend™ Peek Interbody System, Transcend™ Nanotec™ Interbody System, Identiti™ Alif Standalone Interbody System, Identiti™ Nanotec™ Alif Standalone Interbody System.
| Device ID | K222028 |
| 510k Number | K222028 |
| Device Name: | IdentiTi™ Porous Ti Interbody System, IdentiTi™ NanoTec™ Interbody System, Transcend™ PEEK Interbody System, Transcend™ NanoTec™ Interbody System, IdentiTi™ ALIF Standalone Interbody System, IdentiTi™ NanoTec™ ALIF Standalone Interbody System |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | Alphatec Spine 1950 Camino Vide Roble Carlsbad, CA 92008 |
| Contact | Neha Mohindroo |
| Correspondent | Neha Mohindroo Alphatec Spine 1950 Camino Vide Roble Carlsbad, CA 92008 |
| Product Code | MAX |
| Subsequent Product Code | OVD |
| Subsequent Product Code | PHM |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-07-11 |
| Decision Date | 2022-10-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IDENTITI 97773609 not registered Live/Pending |
Identiti Resources, Ltd. 2023-01-30 |
![]() IDENTITI 88469099 not registered Live/Pending |
Identiti Resources, Ltd. 2019-06-11 |
![]() IDENTITI 77343392 3556238 Live/Registered |
ISON DISTRIBUTION, LTD 2007-12-04 |