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iTotal Posterior Stabilized (PS) Knee Replacement System, iTotal Cruciate Retaining (CR) Knee Replacement System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160025
510(k) Type
Special
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2016
Days to Decision
61 days
Submission Type
Summary

iTotal Posterior Stabilized (PS) Knee Replacement System, iTotal Cruciate Retaining (CR) Knee Replacement System

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160025
510(k) Type
Special
Applicant
Conformis, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/2016
Days to Decision
61 days
Submission Type
Summary