MODIFICATION TO REBOUND HRD


Device Classification Name

mesh, surgical, polymeric

510(k) Number K080393
Device Name MODIFICATION TO REBOUND HRD
Applicant
MINNESOTA MEDICAL DEVELOPMENT, INC.
4050 olson memorial highway
suite 350
minneapolis, 
MN 
55422

Applicant Contact julie bulver
Correspondent
MINNESOTA MEDICAL DEVELOPMENT, INC.
4050 olson memorial highway
suite 350
minneapolis, 
MN 
55422

Correspodent Contact julie bulver
Regulation Number 878.3300
Classification Product Code
FTL  
Date Received 02/13/2008
Decision Date 03/13/2008
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