Class Class II

NextAR(TM) Shoulder Platform (K251737)

K251737 2025-09-04 Traditional
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Description

NextAR(TM) Shoulder Platform by Medacta International S.A., an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251737
Clearance Date2025-09-04
Clearance TypeTraditional
Product CodeSBF
Regulation Number882.4560

Categories

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