The following data is part of a premarket notification filed by Alphatec Spine, Inc. with the FDA for Alphatec Navigation Instruments.
Device ID | K153603 |
510k Number | K153603 |
Device Name: | Alphatec Navigation Instruments |
Classification | Orthopedic Stereotaxic Instrument |
Applicant | ALPHATEC SPINE, INC. 5818 EL CAMINO REAL Carlsbad, CA 92008 |
Contact | Renee Murphy |
Correspondent | Renee Murphy ALPHATEC SPINE, INC. 5818 EL CAMINO REAL Carlsbad, CA 92008 |
Product Code | OLO |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-12-17 |
Decision Date | 2016-04-29 |
Summary: | summary |