Class Class II

aprevo® transforaminal lumbar interbody fusion device (K231140)

K231140 2023-05-19 Special
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Description

aprevo® transforaminal lumbar interbody fusion device by Carlsmed, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK231140
Clearance Date2023-05-19
Clearance TypeSpecial
Product CodeMAX
Regulation Number888.3080

Categories

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