Paonan Biotech Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K220261 | NEST-C Interbody System | April 24, 2023 |
| K182285 | PK High Tibial Osteotomy Correction System | June 20, 2019 |
| K180230 | NEST Interbody System | January 25, 2019 |
| K180228 | II-Type Intervertebral Spacer | January 11, 2019 |
| K180226 | TREND II Spinal Fixation System- STEP Series | July 25, 2018 |
| K161225 | Paonan Armstrong Posterior Spinal Fixation System | August 11, 2017 |