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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