← FDA Medical Device Classifications
Intervertebral Fusion Device With Bone Graft, Lumbar
MAX · Class II — Moderate Risk (510(k) clearance required) · Orthopedic · 21 CFR 888.3080
Classification
- FDA Product Code
MAX- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 888.3080
- Review panel
- OR
- Medical specialty
- Orthopedic
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- Y
- Third-party review
- N
Definition
Intended to stabilize spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.
Market data
- Cleared 510(k) submissions
- 886
- Registered establishments
- 417
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown