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

NUVASIVE NEUROVISION JJB SYSTEM

K Number: K032083 · Decision Oct 24, 2003
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
96
Applicant Total
91
Review Days
109

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Basic Information

Device Name
NUVASIVE NEUROVISION JJB SYSTEM
K Number
K032083
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
July 7, 2003
Decision Date
October 24, 2003
Product Code
ETN
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
ETN Stimulator, Nerve

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