Class Class II

Endoskeleton™ Interbody Systems (K251444)

K251444 2025-09-04 Traditional
Home/ Devices/ Endoskeleton™ Interbody Systems (K251444)

Description

Endoskeleton™ Interbody Systems by Medtronic Sofamor Danek USA, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251444
Clearance Date2025-09-04
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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