FDA 510(k) Applications for Medical Device Product Code "KQX"
(Goniometer, Ac-Powered)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K961212 | FASSTECH | SPINAL TOUCH | 06/12/1996 |
| K971079 | INTERLOGICS, INC. | INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE | 07/09/1997 |
| K011827 | ORTHOSCAN LTD. | ORTELIUS 800 | 08/28/2001 |
| K962377 | SKILL TECHNOLOGIES, INC. | 3D-SPINE | 09/03/1996 |
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