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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 K050332
Device Name SURGI-WRAP MAST BIORESORBABLE SHEET
Applicant
MAST BIOSURGERY USA INC.
6749 TOP GUN ST., SUITE C
SAN DIEGO,  CA  92121
Applicant Contact KENNETH K KLEINHENZ
Correspondent
MAST BIOSURGERY USA INC.
6749 TOP GUN ST., SUITE C
SAN DIEGO,  CA  92121
Correspondent Contact KENNETH K KLEINHENZ
Regulation Number878.3300
Classification Product Code
FTL  
Date Received02/10/2005
Decision Date 05/27/2005
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
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