510(k) K223709 ยท HRX Arthroscope
Kyphoplasty Balloon Catheter
| Applicant | Jiangsu Changmei Medtech Co., Ltd., Changzhou, CN |
| Decision | Substantially Equivalent, Aug 16, 2023 |
| Received | Dec 12, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223709
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.