LBM
- Product code
- LBM
- Device name
- Porous Polyethylene Ossicular Replacement
- Device class
- Class 2
- 21 CFR
- 21 CFR 874.3450
- Medical specialty
- Ear, Nose, Throat
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 2
Official FDA classification page: LBM
Classification and pathway per current FDA publications. Data from openFDA (CC0).