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FDA 510(k) Applications for Medical Device Product Code "OJB"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K051821 | INION LTD. | INION S-1 BIODEGRADABLE ANTERIOR CERVICAL FUSION SYSTEM | 11/25/2005 |
K071810 | INION LTD. | INION SPINAL GRAFT CONTAINMENT SYSTEM | 07/11/2008 |
K151360 | Inion Oy | Inion Spinal Graft Containment System | 10/06/2015 |