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 |