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iTotal Identity Cruciate Retaining (CR) Total Knee Replacement, iTotal Identity Posterior Stabilizing (PS) Total Knee Replacement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203447
510(k) Type
Special
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2020
Days to Decision
29 days
Submission Type
Summary

iTotal Identity Cruciate Retaining (CR) Total Knee Replacement, iTotal Identity Posterior Stabilizing (PS) Total Knee Replacement

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203447
510(k) Type
Special
Applicant
Conformis Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2020
Days to Decision
29 days
Submission Type
Summary