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Optetrak Advanced Patella

Page Type
Cleared 510(K)
510(k) Number
K160484
510(k) Type
Special
Applicant
EXACTECH INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2016
Days to Decision
25 days
Submission Type
Summary

Optetrak Advanced Patella

Page Type
Cleared 510(K)
510(k) Number
K160484
510(k) Type
Special
Applicant
EXACTECH INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/2016
Days to Decision
25 days
Submission Type
Summary