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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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