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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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