Micrus Endovascular Corporation - FDA 510(k) Cleared Devices
Recent clearances: MICRUS ASCENT OCCLUSION BALLOON CATHETER 4X7 MM, MICRUS ONE 2 ONE GUIDEWIRE, MICRUS ONE 2 ONE SOFT GUIDEWIRE, MICRUS MICROCATHETER, MODEL COURIER 270
23
Total
23
Cleared
0
Denied
FDA 510(k) Regulatory Record - Micrus Endovascular Corporation Neurology ✕
11 devices
Cleared
Jan 02, 2009
MICRUS MICROCOLI SYSTEM, DELTAPLUSH, MODELS CPL, DPL
Neurology
24d
Cleared
Oct 17, 2008
MICRUS MICROCOIL DELIVERY SYSTEM
Neurology
29d
Cleared
Jun 30, 2008
MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 STRETCH RESISTANT
Neurology
138d
Cleared
May 08, 2008
MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF
Neurology
83d
Cleared
Feb 26, 2008
MICRUS MICROCOIL SYSTEMS
Neurology
81d
Cleared
Oct 05, 2007
MICRUS MICROCOIL SYSTEM CASHMERE-CERECYTE, MODEL CRC
Neurology
60d
Cleared
Jun 01, 2007
MICRUS MICROCOIL DELIVERY SYSTEM, MODELS SPH, HEL, CHE, PC4, HSR, FSR, CSP,...
Neurology
29d
Cleared
Apr 06, 2007
MICRUS MICROCOIL SYSTEM
Neurology
23d
Cleared
Jan 17, 2007
MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC
Neurology
40d
Cleared
Aug 25, 2006
MICRUS MICROCOIL SYSTEM PRESIDIO-18, MODEL PC4
Neurology
37d
Cleared
Dec 07, 2005
MICRUS MODIFIED MICROCOIL 18-SYSTEM, CERECYTE, MODEL CSP & CHE
Neurology
23d