K201139 is an FDA 510(k) clearance for the WEGO-PDO Barbed Suture, a Suture, Surgical, Absorbable, Polydioxanone (Class II — Special Controls, product code NEW), submitted by Foosin Medical Supplies Inc., Ltd. (Weihai, CN). The FDA issued a Cleared decision on October 20, 2020, 175 days after receiving the submission on April 28, 2020. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4840.
| 510(k) Number | K201139 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 28, 2020 |
| Decision Date | October 20, 2020 |
| Days to Decision | 175 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | NEW — Suture, Surgical, Absorbable, Polydioxanone |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4840 |