Last synced on 25 January 2026 at 3:41 am

Identity Imprint Knee Replacement System (including Identity Imprint Posterior Stabilized (PS) KRS and Identity Imprint Cruciate Retaining (CR) KRS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221404
510(k) Type
Traditional
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2022
Days to Decision
71 days
Submission Type
Summary

Identity Imprint Knee Replacement System (including Identity Imprint Posterior Stabilized (PS) KRS and Identity Imprint Cruciate Retaining (CR) KRS)

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221404
510(k) Type
Traditional
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/26/2022
Days to Decision
71 days
Submission Type
Summary