MBP
- Product code
- MBP
- Device name
- Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3045
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 1
- Summaries archived here
- 0 (direct download)
- 510(k) clearances (all years, FDA)
- 31 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K242799 | 2024-11-21 | Lifenet Health | PliaFX Flo | FDA |
Official FDA classification page: MBP
Classification and pathway per current FDA publications. Data from openFDA (CC0).