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 |