The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Anchor Tissue Retrieval System.
| Device ID | K172940 |
| 510k Number | K172940 |
| Device Name: | ANCHOR Tissue Retrieval System |
| 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 | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-26 |
| Decision Date | 2017-10-18 |
| Summary: | summary |