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U.S. Department of Health and Human Services

Product Classification

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Device intervertebral fusion device with bone graft, cervical
Regulation Description Intervertebral body fusion device.
Definition Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.
Physical State Hollow cylinder or rectangular box made of metal or polymer.
Technical Method Acts as a disc spacer and holds bone graft.
Target Area Intervertebral disc space.
Regulation Medical Specialty Orthopedic
Review Panel Orthopedic
Product CodeODP
Premarket Review Office of Orthopedic Devices (OHT6)
Spinal Devices (DHT6B)
Submission Type 510(k)
Regulation Number 888.3080
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Implanted Device? Yes
Life-Sustain/Support Device? No
Recognized Consensus Standards
Third Party Review Not Third Party Eligible