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

NUVASIVE NVM5 SYSTEM

K Number: K123307 · Decision Apr 23, 2013
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
34
Applicant Total
91
Review Days
181

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Basic Information

Device Name
NUVASIVE NVM5 SYSTEM
K Number
K123307
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.1820
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nuvasive, Inc.
Date Received
October 24, 2012
Decision Date
April 23, 2013
Product Code
PDQ
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PDQ Neurosurgical Nerve Locator

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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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