← FDA Medical Device Classifications
Orthosis, Spine, Plate, Laminoplasty, Metal
NQW · Class II — Moderate Risk (510(k) clearance required) · Orthopedic · 21 CFR 888.3050
Classification
- FDA Product Code
NQW- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 888.3050
- Review panel
- OR
- Medical specialty
- Orthopedic
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- Y
- Third-party review
- N
Definition
This device is a plate that is attached to the lamina after a laminoplasty or laminectomy procedure.
Market data
- Cleared 510(k) submissions
- 29
- Registered establishments
- 68
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown