FDA 510(k) Applications Submitted by Conformis Inc

FDA 510(k) Number Submission Date Device Name Applicant
K231178 04/26/2023 ACTERAÖ hip system Conformis Inc
K232426 08/11/2023 Identity Imprint Porous Cruciate Retaining (CR) Knee Replacement System (KRS) with Cruciate Sacrificing (CS) Inserts Conformis Inc


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