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510(k) K191812

ADI Cervical Interbody Fusion Device by Additive Device, Inc. (Adi) D/B/A Restor3D — Product Code ODP

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 24, 2019
Date Received
July 5, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Intervertebral Fusion Device With Bone Graft, Cervical
Device Class
Class II
Regulation Number
888.3080
Review Panel
OR
Submission Type

Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.

Other clearances by Additive Device, Inc. (Adi) D/B/A Restor3D

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