Class Class II

FX V135(TM) Shoulder Prosthesis (K223801)

K223801 2023-06-05 Traditional
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Description

FX V135(TM) Shoulder Prosthesis by Fx Shoulder USA, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223801
Clearance Date2023-06-05
Clearance TypeTraditional
Product CodePHX
Regulation Number888.3660

Categories

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