Class Class II

Huvex Interspinous Fusion System (K223790)

K223790 2023-03-09 Traditional
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Description

Huvex Interspinous Fusion System by Dio Medical Corp. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223790
Clearance Date2023-03-09
Clearance TypeTraditional
Product CodePEK
Regulation Number888.3050

Categories

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