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iTotal Identity Cruciate Retaining (CR) Knee Replacement System, iTotal Identity Posterior Stabilizing (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
K210252
510(k) Type
Special
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2021
Days to Decision
19 days
Submission Type
Summary

iTotal Identity Cruciate Retaining (CR) Knee Replacement System, iTotal Identity Posterior Stabilizing (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
K210252
510(k) Type
Special
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/17/2021
Days to Decision
19 days
Submission Type
Summary