FDA 510(k) Applications Submitted by KATHY BOGGS

FDA 510(k) Number Submission Date Device Name Applicant
K230295 02/02/2023 ATTUNE« Revision Cones DePuy Ireland UC
K101433 05/21/2010 DEPUY ATTUNE KNEE SYSTEM DEPUY ORTHOPAEDICS, INC.
K232303 08/01/2023 ATTUNE« Porous Fixed Bearing Tibial Base, Medialized Dome Patella and Medialized Anatomic Patella with AFFIXIUMÖ 3DP Technology DePuy Ireland UC


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