LGH
- Product code
- LGH
- Device name
- Instrument, Cast Removal, Ac-Powered
- Device class
- Class 1
- 21 CFR
- 21 CFR 888.5960
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K) Exempt
- 510(k) clearances (last 3 years)
- 9
Official FDA classification page: LGH
Classification and pathway per current FDA publications. Data from openFDA (CC0).