MEDTRONIC(R)THRUFLEX(TM) II OVER-THE-WIRE
FDA premarket approval P870036/S018 · decided 1992-12-29
Approval details
- PMA number
- P870036
- Supplement
- S018
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- MEDTRONIC(R)THRUFLEX(TM) II OVER-THE-WIRE
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Applicant
- Medtronics Interventional Vascular
- Date received
- 1992-05-26
- Decision date
- 1992-12-29
- Days to decision
- 217 days
- Decision code
- APPR
- Product code
- LOX
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Santa Rosa, CA
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS (K990707) | Medtronics Interventional Vascular | 1999-03-22 |
| MEDTRONIC ANGIOGRAPHIC CATHETER (K980973) | Medtronics Interventional Vascular | 1998-12-10 |
| MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER (K982883) | Medtronics Interventional Vascular | 1998-09-04 |
| MEDTRONIC ZUMA GUIDING CATHETER (K981198) | Medtronics Interventional Vascular | 1998-08-07 |
| MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE GUIDE WIRE/STANDARD GUIDE WIRE/EXTRA SUPPORT (K972944) | Medtronics Interventional Vascular | 1997-11-03 |
| MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX) (K961917) | Medtronics Interventional Vascular | 1996-11-20 |
| MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT (K960983) | Medtronics Interventional Vascular | 1996-05-30 |
| MEDTRONIC SHERPA GUIDING CATHETER (K955651) | Medtronics Interventional Vascular | 1996-01-22 |