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

Proximity Anterior Cervical Plate System; Segmental Plating System (SPS)

K Number: K251965 · Decision Aug 28, 2025
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
93
Review Days
63

Basic Information

Device Name
Proximity Anterior Cervical Plate System; Segmental Plating System (SPS)
K Number
K251965
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Alphatec Spine, Inc.
Date Received
June 26, 2025
Decision Date
August 28, 2025
Product Code
KWQ
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

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