K192720 is an FDA 510(k) clearance for the GIA Stapler with Tri-Staple Technology, a Staple, Implantable (Class II — Special Controls, product code GDW), submitted by Covidien (Min Hang District, Shanghai, CN). The FDA issued a Cleared decision on March 13, 2020, 168 days after receiving the submission on September 27, 2019. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4750.
| 510(k) Number | K192720 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 27, 2019 |
| Decision Date | March 13, 2020 |
| Days to Decision | 168 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 |