Class Class II

Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft (K251193)

K251193 2025-06-12 Traditional
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Description

Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft by Medtronic Sofamor Danek, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251193
Clearance Date2025-06-12
Clearance TypeTraditional
Product CodeMQV
Regulation Number888.3045

Categories

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