The following data is part of a premarket notification filed by Medtronic Inc. with the FDA for Pacific Xtreme Ptca Balloon Dilatation Catheter.
| Device ID | K103464 |
| 510k Number | K103464 |
| Device Name: | PACIFIC XTREME PTCA BALLOON DILATATION CATHETER |
| Classification | Catheter, Angioplasty, Peripheral, Transluminal |
| Applicant | MEDTRONIC INC. 37A CHERRY HILL DRIVE Danvers, MA 01923 |
| Contact | Heather Morose |
| Correspondent | Heather Morose MEDTRONIC INC. 37A CHERRY HILL DRIVE Danvers, MA 01923 |
| Product Code | LIT |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-11-24 |
| Decision Date | 2010-12-22 |
| Summary: | summary |