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

ARx® SAI Implant System

K Number: K254274 · Decision Apr 16, 2026
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
84
Review Days
107

Basic Information

Device Name
ARx® SAI Implant System
K Number
K254274
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Life Spine, Inc.
Date Received
December 30, 2025
Decision Date
April 16, 2026
Product Code
NKB
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
NKB Thoracolumbosacral Pedicle Screw System

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