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Exactech® TRULIANT® Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240393
510(k) Type
Traditional
Applicant
Exactech Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2024
Days to Decision
238 days
Submission Type
Summary

Exactech® TRULIANT® Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240393
510(k) Type
Traditional
Applicant
Exactech Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2024
Days to Decision
238 days
Submission Type
Summary