The following data is part of a premarket notification filed by Lexington Medical, Inc. with the FDA for Aeon Endoscopic Stapler.
| Device ID | K182380 |
| 510k Number | K182380 |
| Device Name: | AEON Endoscopic Stapler |
| Classification | Staple, Implantable |
| Applicant | Lexington Medical, Inc. 11 Executive Park Drive Billerica, MA 01862 |
| Contact | Douglas Macbride |
| Correspondent | Douglas Macbride Lexington Medical, Inc. 11 Executive Park Drive Billerica, MA 01862 |
| Product Code | GDW |
| CFR Regulation Number | 878.4750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-08-31 |
| Decision Date | 2018-11-28 |
| Summary: | summary |