K190331 is an FDA 510(k) clearance for the Applied Medical Laparoscopic Linear Cutter. This device is classified as a Staple, Implantable (Class II - Special Controls, product code GDW).
Submitted by Applied Medical Resources Corporation (Rancho Santa, US). The FDA issued a Cleared decision on November 22, 2019, 281 days after receiving the submission on February 14, 2019.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4750.
| 510(k) Number | K190331 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | February 14, 2019 |
| Decision Date | November 22, 2019 |
| Days to Decision | 281 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | GDW — Staple, Implantable |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4750 |