Class Class II

PEEK SA Anterior Lumbar Interbody Fusion (ALIF) System (K230808)

K230808 2023-04-21 Special
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Description

PEEK SA Anterior Lumbar Interbody Fusion (ALIF) System by Kyocera Medical Technologies, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230808
Clearance Date2023-04-21
Clearance TypeSpecial
Product CodeOVD
Regulation Number888.3080

Categories

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