K241014 is an FDA 510(k) clearance for the Biomet Kirschner Wires (K-Wires). This device is classified as a Pin, Fixation, Smooth (Class II - Special Controls, product code HTY).
Submitted by Biomet, Inc. (Warsaw, US). The FDA issued a Cleared decision on May 22, 2024, 40 days after receiving the submission on April 12, 2024.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K241014 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 12, 2024 |
| Decision Date | May 22, 2024 |
| Days to Decision | 40 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | HTY — Pin, Fixation, Smooth |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3040 |