PARIETEX PROGRIP


Device Classification Name

mesh, surgical, polymeric

510(k) Number K103682
Device Name PARIETEX PROGRIP
Applicant
SOFRADIM PRODUCTION
15 crosby drive
bedford, 
MA 
01730

Applicant Contact james mcmahon
Correspondent
SOFRADIM PRODUCTION
15 crosby drive
bedford, 
MA 
01730

Correspodent Contact james mcmahon
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 12/17/2010
Decision Date 03/04/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No