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FDA 510(k) Applications Submitted by MIMEDX GROUP, INC
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100905
04/01/2010
HYDROFIX SURGICAL SHEET
MIMEDX GROUP, INC
K100313
02/04/2010
HYDROFIX SURGICAL SHEET
MIMEDX GROUP, INC
K101805
06/28/2010
HYDROFIX VASO SHIELD
MIMEDX GROUP, INC
K101826
07/01/2010
HYDROFIX VASO SHIELD, MODEL HVS-001-0610
MIMEDX GROUP, INC
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