K240035 is an FDA 510(k) clearance for the TACTIX Vector Syndesmosis System. This device is classified as a Washer, Bolt Nut (Class II - Special Controls, product code HTN).
Submitted by Vilex, LLC (Mcminnville, US). The FDA issued a Cleared decision on August 1, 2024, 210 days after receiving the submission on January 4, 2024.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.
| 510(k) Number | K240035 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 04, 2024 |
| Decision Date | August 01, 2024 |
| Days to Decision | 210 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | HTN - Washer, Bolt Nut |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |