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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer
510(k) Number K221404
Device Name Identity Imprint Knee Replacement System (including Identity Imprint Posterior Stabilized (PS) KRS and Identity Imprint Cruciate Retaining (CR) KRS)
Applicant
Conformis Inc.
600 Technology Park Drive, 4th Floor
Billerica,  MA  01821
Applicant Contact Mary Kruitwagen
Correspondent
Conformis Inc.
600 Technology Park Drive, 4th Floor
Billerica,  MA  01821
Correspondent Contact Kara Johnson
Regulation Number888.3560
Classification Product Code
JWH  
Subsequent Product Codes
OIY   OOG  
Date Received05/16/2022
Decision Date 07/26/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Orthopedic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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