The following data is part of a premarket notification filed by Ev3 Corporation with the FDA for Protege Rx Gps Self-expanding Nitrinol Stent.
| Device ID | K051379 |
| 510k Number | K051379 |
| Device Name: | PROTEGE RX GPS SELF-EXPANDING NITRINOL STENT |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | EV3 CORPORATION 4600 NATHAN LN. NORTH Plymouth, MN 55442 -2920 |
| Contact | Glen D Smythe |
| Correspondent | Glen D Smythe EV3 CORPORATION 4600 NATHAN LN. NORTH Plymouth, MN 55442 -2920 |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Se - With Limitations (SESU) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-05-27 |
| Decision Date | 2005-06-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00821684032220 | K051379 | 000 |