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Intervertebral Fusion Device With Bone Graft, Thoracic

FDA product code PHM · 2 cleared devices

Class 2 Orthopedic
Regulation
21 CFR 888.3080
Review panel
OR
Implant
Yes
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2016-09-08 – 2018-05-31

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

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