K190166 is an FDA 510(k) clearance for the TriMed Nitinol Staple System. This device is classified as a Staple, Fixation, Bone (Class II - Special Controls, product code JDR).
Submitted by TriMed, Inc. (Santa Clarita, US). The FDA issued a Cleared decision on July 1, 2019, 151 days after receiving the submission on January 31, 2019.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3030.
| 510(k) Number | K190166 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 31, 2019 |
| Decision Date | July 01, 2019 |
| Days to Decision | 151 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | JDR - Staple, Fixation, Bone |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3030 |