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Synovis Life Technologies. Inc. (A Subsidiary of Baxter

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K213125 PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP TechnologyFTM2021-10-27 View
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