Class Class II

Arthrex Virtual Implant Positioning (VIP) System (K222007)

K222007 2023-03-08 Traditional
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Description

Arthrex Virtual Implant Positioning (VIP) System by Arthrex, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222007
Clearance Date2023-03-08
Clearance TypeTraditional
Product CodeQHE
Regulation Number888.3660

Categories

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