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

NUVASIVE SAGE LATERAL PLATE SYSTEM

K Number: K121815 · Decision Oct 23, 2012
Classifications
1
FEI Numbers
356
Registration Numbers
356
Same Product Code
665
Applicant Total
91
Review Days
125

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Basic Information

Device Name
NUVASIVE SAGE LATERAL PLATE SYSTEM
K Number
K121815
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3060
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuvasive, Inc.
Date Received
June 20, 2012
Decision Date
October 23, 2012
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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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
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