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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name mesh, surgical, polymeric
510(k) Number K083467
Device Name REBOUND HRDV
Applicant
MINNESOTA MEDICAL DEVELOPMENT, INC.
14305 21ST AVE. NORTH
SUITE 100
PLYMOUTH,  MN  55447
Applicant Contact STEVE NUSS
Correspondent
MINNESOTA MEDICAL DEVELOPMENT, INC.
14305 21ST AVE. NORTH
SUITE 100
PLYMOUTH,  MN  55447
Correspondent Contact STEVE NUSS
Regulation Number878.3300
Classification Product Code
FTL  
Date Received11/24/2008
Decision Date 04/23/2009
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
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