Class Class II

Solar™ Lumbar Interbody Fusion System (K240326)

K240326 2024-07-29 Traditional
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Description

Solar™ Lumbar Interbody Fusion System by Degen Medical, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240326
Clearance Date2024-07-29
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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