Joimax GmbH - FDA 510(k) Cleared Devices
Recent clearances: EndoLIF Delta-Cage and DoubleWedge-Cage, Joimax Intracs System, Percusys® Plus Pedicle Screw System
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Joimax GmbH General & Plastic Surgery ✕
2 devices