K170716 is an FDA 510(k) clearance for the PercuNav Image Fusion and Interventional Navigation. This device is classified as a System, X-ray, Tomography, Computed (Class II - Special Controls, product code JAK).
Submitted by Philips Ultrasound, Inc. (Andover, US). The FDA issued a Cleared decision on April 21, 2017, 43 days after receiving the submission on March 9, 2017.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1750.
| 510(k) Number | K170716 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 09, 2017 |
| Decision Date | April 21, 2017 |
| Days to Decision | 43 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | JAK - System, X-ray, Tomography, Computed |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1750 |