Class Class II

Balanced Knee System TriMax Porous Femoral Components (K253161)

K253161 2025-12-19 Traditional
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Description

Balanced Knee System TriMax Porous Femoral Components by Ortho Development Corp., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253161
Clearance Date2025-12-19
Clearance TypeTraditional
Product CodeMBH
Regulation Number888.3565

Categories

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