K202307 is an FDA 510(k) clearance for the Activ Fuse. This device is classified as a Plate, Fixation, Bone (Class II - Special Controls, product code HRS).
Submitted by Newclip Technics (Haute-Goulaine, FR). The FDA issued a Cleared decision on November 17, 2020, 95 days after receiving the submission on August 14, 2020.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.
| 510(k) Number | K202307 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 14, 2020 |
| Decision Date | November 17, 2020 |
| Days to Decision | 95 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | HRS — Plate, Fixation, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |