JDW
- Product code
- JDW
- Device name
- Pin, Fixation, Threaded
- Device class
- Class 2
- 21 CFR
- 21 CFR 888.3040
- Medical specialty
- Orthopedic
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 3
- Summaries archived here
- 3 (direct download)
- 510(k) clearances (all years, FDA)
- 94 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (3)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K260073 | 2026-02-10 | Biodynamik, Inc. | XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 … | |
| K250316 | 2025-10-29 | Meduloc, LLC | Meduloc Intramedullary Fracture Fixation (IFF) Syste… | |
| K241357 | 2025-01-22 | Biodynamik, Inc. | XT3 System |
Official FDA classification page: JDW
Classification and pathway per current FDA publications. Data from openFDA (CC0).