Last synced on 14 November 2025 at 11:06 pm

Balanced Knee Revision System Trabecular Tibial Cone Augments

Page Type
Cleared 510(K)
510(k) Number
K182085
510(k) Type
Traditional
Applicant
Ortho Development Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2018
Days to Decision
90 days
Submission Type
Summary

Balanced Knee Revision System Trabecular Tibial Cone Augments

Page Type
Cleared 510(K)
510(k) Number
K182085
510(k) Type
Traditional
Applicant
Ortho Development Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2018
Days to Decision
90 days
Submission Type
Summary