FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SafeOp 3: Neural Informatix System

K Number: K252842 · Decision Jan 11, 2026
Classifications
1
FEI Numbers
88
Registration Numbers
88
Same Product Code
138
Applicant Total
93
Review Days
125

Basic Information

Device Name
SafeOp 3: Neural Informatix System
K Number
K252842
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1870
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alphatec Spine, Inc.
Date Received
September 8, 2025
Decision Date
January 11, 2026
Product Code
GWF
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWF Stimulator, Electrical, Evoked Response

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