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

MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE

K Number: K071300 · Decision Jul 20, 2007
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
62
Applicant Total
423
Review Days
72

Basic Information

Device Name
MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE
K Number
K071300
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4725
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SMITH & NEPHEW, INC.
Date Received
May 9, 2007
Decision Date
July 20, 2007
Product Code
GXI
Advisory Committee
Neurology
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
GXI Probe, Radiofrequency Lesion

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