K232251 is an FDA 510(k) clearance for the APTUS Cannulated Compression Screws Line Extension, APTUS K-Wire System Line Extension. This device is classified as a Screw, Fixation, Bone (Class II - Special Controls, product code HWC).
Submitted by Medartis AG (Basel, CH). The FDA issued a Cleared decision on November 3, 2023, 98 days after receiving the submission on July 28, 2023.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K232251 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 28, 2023 |
| Decision Date | November 03, 2023 |
| Days to Decision | 98 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | HWC — Screw, Fixation, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3040 |