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FDA 510(k) Application Details - K080393
Device Classification Name
Mesh, Surgical, Polymeric
More FDA Info for this Device
510(K) Number
K080393
Device Name
Mesh, Surgical, Polymeric
Applicant
MINNESOTA MEDICAL DEVELOPMENT, INC.
4050 OLSON MEMORIAL HIGHWAY
SUITE 350
MINNEAPOLIS, MN 55422 US
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Contact
JULIE BULVER
Other 510(k) Applications for this Contact
Regulation Number
878.3300
More FDA Info for this Regulation Number
Classification Product Code
FTL
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More FDA Info for this Product Code
Date Received
02/13/2008
Decision Date
03/13/2008
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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