Last synced on 14 November 2025 at 11:06 pm

ITOTAL POSTERIOR STABILIZED (PS) KNEE REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140833
510(k) Type
Traditional
Applicant
CONFORMIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2014
Days to Decision
89 days
Submission Type
Summary

ITOTAL POSTERIOR STABILIZED (PS) KNEE REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K140833
510(k) Type
Traditional
Applicant
CONFORMIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2014
Days to Decision
89 days
Submission Type
Summary