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

SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline™ System

K Number: K253739 · Decision May 7, 2026
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
172
Review Days
164

Basic Information

Device Name
SCRIPT™ Rods, CREO™ Stabilization System, REVERE® Stabilization System, REVERE® 4.5 Stabilization System, NuVasive Reline™ System
K Number
K253739
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Globus Medical, Inc.
Date Received
November 24, 2025
Decision Date
May 7, 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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