Rebound Therapeutics
Rebound Therapeutics appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 2, 2021.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K203745 | AURORA Evacuator +Coag | December 2, 2021 |
| K201840 | Aurora Surgiscope System (Surgiscope), Aurora Surgiscope System (Image Control Box) | November 4, 2020 |
| K201637 | Aurora Evacuator +Coag | August 12, 2020 |
| K191861 | Aurora Surgiscope System | December 6, 2019 |
| K190075 | Aurora Evacuator | February 12, 2019 |
| K180372 | Aurora Evacuator | April 9, 2018 |