FDA 510(k) Applications for Medical Device Product Code "ORR"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K171257 | MRI Interventions, Inc. | ClearPoint System | 10/20/2017 |
| K181195 | MRI Interventions, Inc. | ClearPoint System | 11/02/2018 |
| K111073 | SURGI-VISION, INC. | SURGIVISION INC. CLEARPOINT SYSTEM | 06/22/2011 |
| K100836 | SURGIVISION, INC. | CLEARPOINT SYSTEM | 06/16/2010 |
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