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Synovis Life Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories2
Latest FDA decision2023-04-07
TypeNumberDevice NameCodeDateActions
510(k) K223052 Peri-Guard and Supple Peri-GuardFTM2023-04-07 View
510(k) K221029 PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair PatchPSQ2022-10-19 View
510(k) K221032 Vascu-Guard Vascular Repair PatchPSQ2022-10-19 View
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