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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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