K182380 is an FDA 510(k) clearance for the AEON Endoscopic Stapler, a Staple, Implantable (Class II — Special Controls, product code GDW), submitted by Lexington Medical, Inc. (Billerica, US). The FDA issued a Cleared decision on November 28, 2018, 89 days after receiving the submission on August 31, 2018. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4750.
| 510(k) Number | K182380 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | August 31, 2018 |
| Decision Date | November 28, 2018 |
| Days to Decision | 89 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 |