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Arthrex iBalance Patella Implant, Dome

Page Type
Cleared 510(K)
510(k) Number
K143047
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2014
Days to Decision
27 days
Submission Type
Summary

Arthrex iBalance Patella Implant, Dome

Page Type
Cleared 510(K)
510(k) Number
K143047
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2014
Days to Decision
27 days
Submission Type
Summary