510(k) K252842

Device
SafeOp 3: Neural Informatix System
Applicant
Alphatec Spine, Inc.
510(k) number
K252842
Product code
GWF
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-11
Date received
2025-09-08
Regulation
882.1870
Classification name
Stimulator, Electrical, Evoked Response
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Garima Shrivastava
Address
1950 Camino Vida Roble Carlsbad CA US 92008 92008

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code GWF

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K242345Delphi StimulatorQuantalx Neuroscience2024-11-05
K234092SafeOp 3: Neural Informatix SysteemAlphatec Spine, Inc.2024-04-19
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K162873MEP MonitorTonica Elektronik A/S2017-03-31