FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

Universal Spinal System

K Number: K252729 · Decision Nov 18, 2025
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
12
Review Days
82

Basic Information

Device Name
Universal Spinal System
K Number
K252729
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Double Medical Technology, Inc.
Date Received
August 28, 2025
Decision Date
November 18, 2025
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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