The following data is part of a premarket notification filed by Alphatec Spine, Inc. with the FDA for Appliance, Fixation, Spinal Intervertebral Body.
| Device ID | K102820 |
| 510k Number | K102820 |
| Device Name: | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | ALPHATEC SPINE, INC. 5818 EL CAMINO REAL Carlsbad, CA 92008 |
| Contact | Karla Schaffner |
| Correspondent | Karla Schaffner ALPHATEC SPINE, INC. 5818 EL CAMINO REAL Carlsbad, CA 92008 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-09-28 |
| Decision Date | 2010-11-05 |
| Summary: | summary |