510(k) K221142 ยท HRX Arthroscope
Kyphoplasty Balloon System
| Applicant | OK Medinet Korea Co., Ltd., Seoul, KR |
| Decision | Substantially Equivalent, Apr 21, 2023 |
| Received | Apr 19, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221142
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.