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

GSB GLOBAL SPINAL BALANCE SYSTEM

K Number: K132014 · Decision Oct 31, 2013
Classifications
1
FEI Numbers
407
Registration Numbers
407
Same Product Code
900
Applicant Total
91
Review Days
122

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
GSB GLOBAL SPINAL BALANCE SYSTEM
K Number
K132014
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuvasive, Inc.
Date Received
July 1, 2013
Decision Date
October 31, 2013
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NKB), ordered by most recent decision date.

View all

Other Clearances by Nuvasive, Inc.

K Number Device Name
K240507 NuVasive AttraX Scaffold
K223731 NuVasive Modulus-C Interbody System
K211757 Simplify Disc
K173117 NuVasive® VersaTie™ System
K141665 NuVasive CoRoent System
K142205 NuVasive X-CORE(R) Expandable VBR System
K141968 NUVASIVE NVM5 SYSTEM
K140319 COROENT TI-C SYSTEM
K140162 AP EXPANDABLE XLIF SYSTEM
K140003 COROENT SMALL INTERBODY SYSTEM
Search all 91 clearances from Nuvasive, Inc. →