Class Class II

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) (K232996)

K232996 2024-09-06 Traditional
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Description

Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) by Shanghai Iatrical-Ti Technologies CO , Ltd. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK232996
Clearance Date2024-09-06
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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