|
Device | CORDIS PTCA DILATATION CATHETER |
Generic Name | Catheters, transluminal coronary angioplasty, percutaneous |
Regulation Number | 870.5100 |
Applicant | CORDIS CORP. 14201 N.W. 60TH AVE. MIAMI LAKES, FL 33014-5700 |
PMA Number | P880003 |
Supplement Number | S092 |
Date Received | 06/15/2007 |
Decision Date | 07/13/2007 |
Reclassified Date
|
10/08/2010 |
Product Code |
LOX |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement CHANGE THE HIGH-DENSITY POLYETHYLENE (HDPE) FORMING TUBE EXTRUSION PROCESS FROM AIR EXTRUSION TO VACUUM EXTRUSION. |