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OPTETRAK TOTAL KNEE SYSTEM, HI-FLEX ASYMMETRIC POSTERIOR-STABILIZED CEMENTED FEMORAL COMPONENTS, HI-FLEX POSTERIOR-STABI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033883
510(k) Type
Special
Applicant
Exactech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2004
Days to Decision
60 days
Submission Type
Summary

OPTETRAK TOTAL KNEE SYSTEM, HI-FLEX ASYMMETRIC POSTERIOR-STABILIZED CEMENTED FEMORAL COMPONENTS, HI-FLEX POSTERIOR-STABI

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033883
510(k) Type
Special
Applicant
Exactech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/13/2004
Days to Decision
60 days
Submission Type
Summary