The following data is part of a premarket notification filed by St. Jude Medical with the FDA for Modification To Proxis System.
| Device ID | K073563 |
| 510k Number | K073563 |
| Device Name: | MODIFICATION TO PROXIS SYSTEM |
| Classification | Temporary Coronary Saphenous Vein Bypass Graft For Embolic Protection |
| Applicant | ST. JUDE MEDICAL 6550 WEDGWOOD RD. NORTH SUITE 150 Maple Grove, MN 55311 |
| Contact | Linh Pham |
| Correspondent | Linh Pham ST. JUDE MEDICAL 6550 WEDGWOOD RD. NORTH SUITE 150 Maple Grove, MN 55311 |
| Product Code | NFA |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-12-19 |
| Decision Date | 2008-01-31 |
| Summary: | summary |