Conventus Orthopaedics
Conventus Orthopaedics appears in FDA public data with 0 recalls, 6 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 22, 2021.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K202858 | Flex-ThreadTM Distal Fibula Intramedullary Nail System | January 22, 2021 |
| K161048 | Conventus Orthopaedics Ulna Fixation System | July 26, 2016 |
| K151379 | Conventus PRS System | August 13, 2015 |
| K141737 | CONVENTUS PHS SYSTEM | April 8, 2015 |
| K131552 | CONVENTUS DRS | February 12, 2014 |
| K102689 | CONVENTUS ORTHOPAEDICS FRACTURE FIXATION SYSTEM | January 17, 2013 |