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FDA 510(k) Applications Submitted by Synovis Life Technologies. Inc. (A Subsidiary Of Baxter
FDA 510(k) Number
Submission Date
Device Name
Applicant
K213125
09/27/2021
PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP Technology
Synovis Life Technologies. Inc. (A Subsidiary Of Baxter
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