K240393
- 510(k) number
- K240393
- Device name
- Exactech® TRULIANT® Knee System
- Applicant
- Exactech, Inc. FL · US
- Product code
- MBH — Prosthesis, Knee, Patello/Femorotibial, Semi-Constra
- Decision date
- 2024-10-03
- Date received
- 2024-02-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K240393.pdf
Official FDA record: K240393
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.