FDA 510(k) Applications Submitted by CONFORMIS, INC

FDA 510(k) Number Submission Date Device Name Applicant
K152704 09/21/2015 iTotal Posterior Stabilized Knee Replacement System, iTotal Cruciate Retaining Knee Replacement System CONFORMIS, INC
K170226 01/25/2017 iTotal Family Reusable Instrument Tray CONFORMIS, INC


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