K203381 is an FDA 510(k) clearance for the Dynanail Mini Hybrid. This device is classified as a Screw, Fixation, Bone (Class II - Special Controls, product code HWC).
Submitted by MedShape, Inc. (Atlanta, US). The FDA issued a Cleared decision on January 15, 2021, 59 days after receiving the submission on November 17, 2020.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3040.
| 510(k) Number | K203381 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | November 17, 2020 |
| Decision Date | January 15, 2021 |
| Days to Decision | 59 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 |