The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Anchor Tissue Retrieval System By Conmed.
| Device ID | K173822 |
| 510k Number | K173822 |
| Device Name: | Anchor Tissue Retrieval System By CONMED |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | Conmed Corporation 525 French Road Utica, NY 13502 |
| Contact | Rachelle D Fitzgerald |
| Correspondent | Rachelle D Fitzgerald Conmed Corporation 525 French Road Utica, NY 13502 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-18 |
| Decision Date | 2018-09-11 |
| Summary: | summary |