FDA 510(k) Applications Submitted by JODI JORGENSON

FDA 510(k) Number Submission Date Device Name Applicant
K122306 08/01/2012 SYNOVIS COLLAGEN MATRIX (TBD) SYNOVIS SURGICAL INNOVATIONS
K142447 09/02/2014 PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair Patch Synovis Life Technologies. Inc.
K142461 09/02/2014 VASCU-GUARD Peripheral Vascular Patch Synovis Life Technologies Inc.
K083039 10/14/2008 VERITAS COLLAGEN MATRIX (DRY) SYNOVIS SURGICAL INNOVATIONS
K143589 12/18/2014 GEM Flow COUPLER Device and System Synovis Life Technologies, Inc.


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