SOPRO 670 ARTHROSCOPIC PUMP


Device Classification Name

arthroscope

510(k) Number K080122
Device Name SOPRO 670 ARTHROSCOPIC PUMP
Applicant
SOPRO
124 gaither drive
suite 140
mt. laurel, 
NJ 
08054

Applicant Contact steve salesky
Correspondent
SOPRO
124 gaither drive
suite 140
mt. laurel, 
NJ 
08054

Correspodent Contact steve salesky
Regulation Number 888.1100
Classification Product Code
HRX  
Date Received 01/17/2008
Decision Date 07/11/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Orthopedic

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No