OrthoGrid Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K260077 | OrthoGrid Hip AI® 4.0 | May 29, 2026 |
| K210136 | PhantomMSK Hip | February 18, 2021 |
| K192279 | PhantomMSK Trauma | December 7, 2019 |
| K182332 | PhantomMSK | February 15, 2019 |