Class Class II

NITRO Interbody Fusion Cage System Family (K220513)

K220513 2023-04-25 Traditional
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Description

NITRO Interbody Fusion Cage System Family by Ctl Medical Corporation — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220513
Clearance Date2023-04-25
Clearance TypeTraditional
Product CodeODP
Regulation Number888.3080

Categories

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