FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Balanced Knee System TriMax Porous Femoral Components

K Number: K253161 · Decision Dec 19, 2025
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
142
Applicant Total
45
Review Days
84

Basic Information

Device Name
Balanced Knee System TriMax Porous Femoral Components
K Number
K253161
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3565
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho Development Corp.
Date Received
September 26, 2025
Decision Date
December 19, 2025
Product Code
MBH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

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