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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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