The following data is part of a premarket notification filed by Boston Scientific Corporation with the FDA for Ultraflex Esophageal Ng Stent System.
| Device ID | K120983 |
| 510k Number | K120983 |
| Device Name: | ULTRAFLEX ESOPHAGEAL NG STENT SYSTEM |
| Classification | Prosthesis, Esophageal |
| Applicant | Boston Scientific Corporation 100 BOSTON SCIENTIFIC WAY Marlborough, MA 01752 |
| Contact | Janis F Taranto |
| Correspondent | Janis F Taranto Boston Scientific Corporation 100 BOSTON SCIENTIFIC WAY Marlborough, MA 01752 |
| Product Code | ESW |
| CFR Regulation Number | 878.3610 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-04-02 |
| Decision Date | 2012-05-02 |
| Summary: | summary |