FDA 510(k) Applications for Medical Device Product Code "HWT"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960685 | INTEGRATED SURGICAL SYSTEMS, INC. | ORTHODOC PREOPERATIVE PLANNER MODEL 500 | 01/17/1997 |
K974406 | ORTHO-GRAPHICS, INC. | ORTHOPLAN | 02/18/1998 |