← FDA Medical Device Classifications
Bone Cement, Posterior Screw Augmentation
PML · Class II — Moderate Risk (510(k) clearance required) · Orthopedic · 21 CFR 888.3027
Classification
- FDA Product Code
PML- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 888.3027
- Review panel
- OR
- Medical specialty
- Orthopedic
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- Y
- Third-party review
- N
Definition
The device is intended to augment the fixation of screws in a posterior spinal system construct.
Market data
- Cleared 510(k) submissions
- 18
- Registered establishments
- 80
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown