LXI
- Product code
- LXI
- Device name
- Guide, Drill, Ligament
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4820
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (all years, FDA)
- 8 (all years; only the last 3 years are listed here)
Official FDA classification page: LXI
Classification and pathway per current FDA publications. Data from openFDA (CC0).