SURGIMESH XB


Device Classification Name

mesh, surgical, polymeric

510(k) Number K072974
Device Name SURGIMESH XB
Applicant
ASPIDE MEDICAL
555 thirteenth st. nw
columbia square
washington, 
DC 
20004 -1109

Applicant Contact howard m holstein
Correspondent
ASPIDE MEDICAL
555 thirteenth st. nw
columbia square
washington, 
DC 
20004 -1109

Correspodent Contact howard m holstein
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 10/22/2007
Decision Date 08/18/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No