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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213389
510(k) Type
Special
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2021
Days to Decision
26 days
Submission Type
Summary

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213389
510(k) Type
Special
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/10/2021
Days to Decision
26 days
Submission Type
Summary