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 |