FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

U2 Total Knee System – PF+ Patella; USTAR II System– PF+ Patella

K Number: K243656 · Decision Jul 31, 2025
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
142
Applicant Total
40
Review Days
247

Basic Information

Device Name
U2 Total Knee System – PF+ Patella; USTAR II System– PF+ Patella
K Number
K243656
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3565
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
United Orthopedic Corporation
Date Received
November 26, 2024
Decision Date
July 31, 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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Other Clearances by United Orthopedic Corporation

K Number Device Name
K252725 Stem Extension Line (U2 Total Knee System—PSA Type)
K252303 Stem Extension Line (USTAR II System)
K242315 Resolve Modular Revision Hip Stem
K243466 Conformity Stem Extension Line, #0
K243024 Cellbrick Knee Spacer
K242249 Conformity Stem Extension Line
K221705 U2 Total Knee System-PF+
K221149 U-Motion II Acetabular System-Extension line
K221675 United U2 femoral head, 22mm delta ceramic head
K222700 Tibial baseplate, Tibial insert
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