Last synced on 25 January 2026 at 3:41 am

Identity Imprint Porous Cruciate Retaining (CR) Knee Replacement System (KRS) with Cruciate Sacrificing (CS) Inserts

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232426
510(k) Type
Special
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2023
Days to Decision
28 days
Submission Type
Summary

Identity Imprint Porous Cruciate Retaining (CR) Knee Replacement System (KRS) with Cruciate Sacrificing (CS) Inserts

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K232426
510(k) Type
Special
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/8/2023
Days to Decision
28 days
Submission Type
Summary