MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE

Device Classification Name

probe, radiofrequency lesion

510(k) Number K071300
Device Name MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE
Applicant
SMITH & NEPHEW, INC.
150 minuteman rd.
andover, 
MA 
01810

Applicant Contact kathy reddig
Correspondent
SMITH & NEPHEW, INC.
150 minuteman rd.
andover, 
MA 
01810

Correspodent Contact kathy reddig
Regulation Number 882.4725
Classification Product Code
GXI  
Date Received 05/09/2007
Decision Date 07/20/2007
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No