← FDA Medical Device Classifications
Materials, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Alveolar Ridge Augmentation
NFE · Class II — Moderate Risk (510(k) clearance required) · Dental · 21 CFR 872.3680
Classification
- FDA Product Code
NFE- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 872.3680
- Review panel
- DE
- Medical specialty
- Dental
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- N
- Implant
- N
- Third-party review
- N
Market data
- Cleared 510(k) submissions
- 0
- Registered establishments
- 0
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown