LXM
- Product code
- LXM
- Device name
- Manipulator, Plunger-Like Joint
- Device class
- Class U
- Medical specialty
- Unknown
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 32
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K234036 | 2024-02-15 | Neuro Spinal Innovation, Inc. | SONIK MONARK 100 |
Official FDA classification page: LXM
Classification and pathway per current FDA publications. Data from openFDA (CC0).