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FDA 510(k) Applications Submitted by Matrix Surgical Holdings, LLC/Matrix Surgical USA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K180249
01/29/2018
OmniPore DUROMAX Surgical Implants
Matrix Surgical Holdings, LLC/Matrix Surgical USA
K133046
09/27/2013
OMNIPORE CUSTOMIZED SURGICAL IMPLANTS
MATRIX SURGICAL HOLDINGS, LLC/MATRIX SURGICAL USA
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