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 |