K193523 is an FDA 510(k) clearance for the ArthrexVIP Web Portal. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).
Submitted by Arthrex, Inc. (Naples, US). The FDA issued a Cleared decision on April 30, 2020, 133 days after receiving the submission on December 19, 2019.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 892.2050.
| 510(k) Number | K193523 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 19, 2019 |
| Decision Date | April 30, 2020 |
| Days to Decision | 133 days |
| Submission Type | Special |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | LLZ — System, Image Processing, Radiological |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.2050 |