Devices · Alphatec Spine, Inc.
SafeOp 3: Neural Informatix System
510(k)K252842NeurologyGWF
Alphatec Spine, Inc. is listed for SafeOp 3: Neural Informatix System (K252842). The FDA list gives January 11, 2026 as the date of the final decision. The lead panel is Neurology, and the database link on the FDA list is the 510(k) pathway. The primary product code on the FDA list is GWF. openFDA did not return a classification record for that code in this copy of the data. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K252842
- Date of final decision
- January 11, 2026
- Company on the FDA list
- Alphatec Spine, Inc.
- Lead panel
- Neurology
- Primary product code
- GWF
- openFDA device name for the code
- Stimulator, Electrical, Evoked Response
- Device class
- 2
- Regulation number
- 882.1870
- openFDA decision description
- Substantially Equivalent
- openFDA decision code
- SESE
- Statement or summary label
- Summary