GALILEO INTRAVASCULAR RADIOTHERAPY SYSTEM
FDA premarket approval P000052/S006 · decided 2002-08-02
Approval details
- PMA number
- P000052
- Supplement
- S006
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- GALILEO INTRAVASCULAR RADIOTHERAPY SYSTEM
- Generic name
- Intravascular radiation delivery system
- Applicant
- Guidant Corp.
- Date received
- 2002-02-22
- Decision date
- 2002-08-02
- Days to decision
- 161 days
- Decision code
- APPR
- Product code
- MOU
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Temecula, CA
- Statement
- APPROVAL FOR CHANGES TO COMPONENTS USED IN THE SDU HEAD AND CARTRIDGE OF THE GALILEO INTRAVASCULAR RADIOTHERAPY SYSTEM. THE DEVICE MODIFICATIONS INCLUDE CHANGES TO THE EMERGENCY RETRACT SYSTEM, THE STOP COLLAR/WIRE DRIVES AND THE CARTRIDGE LATCHING MECHANISM.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| FLEX 10 MIS ABLATION PROBE, MODEL FLX10MI-05 (K061865) | Guidant Corp. | 2006-07-27 |
| HI-TORQUE WHISPER VIEW GUIDE WIRE (K061453) | Guidant Corp. | 2006-06-22 |
| RX ACCUNET 2 EMBOLIC PROTECTION SYSTEM (K042908) | Guidant Corp. | 2004-11-12 |
| ACCUNET EMBOLIC PROTECTION SYSTEM, RX ACCUNET EMBOLIC PROTECTION SYSTEM (K042218) | Guidant Corp. | 2004-08-31 |
| OMNILINK .018 BILIARY STENT SYSTEM (K033834) | Guidant Corp. | 2004-01-02 |
| ABSOLUTE .035 SELF-EXPANDING BILIARY STENT SYSTEM (K033393) | Guidant Corp. | 2003-11-10 |
| HI-TORQUE BALANCE INIVERSAL GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING (K031678) | Guidant Corp. | 2003-08-26 |
| RAPIDO CUT-AWAY CUTTER (K031459) | Guidant Corp. | 2003-07-23 |