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Parker Quality & Compliance

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510(k) clearance

Unity Total Knee System, Unity Knee Cementless CR Femur

FDA 510(k) source

510(k) number
K261275
Applicant
Corin, Ltd.
Decision date
Sep 17, 2026
Date received
Apr 17, 2026
Decision
Substantially Equivalent
Clearance type
Traditional
Product code
MBH
Device type
Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
Device class
Class II
Regulation
21 CFR 888.3565
Advisory committee
Orthopedic
Statement or summary
Summary
Third party
N
Location
Cirencester, GB