SUPRAMESH EXTRA


Device Classification Name

mesh, surgical, polymeric

510(k) Number K080216
Device Name SUPRAMESH EXTRA
Applicant
S. JACKSON, INC.
9109 coperhaver dr
potomac, 
MD 
20854

Applicant Contact norman r estrin
Correspondent
S. JACKSON, INC.
9109 coperhaver dr
potomac, 
MD 
20854

Correspodent Contact norman r estrin
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 01/29/2008
Decision Date 09/15/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No