Micrus Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Micrus Corp. Neurology ✕
5 devices
Cleared
Feb 04, 2004
MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE
Neurology
57d
Cleared
Nov 28, 2003
MICRUS MICROCOIL SYSTEM
Neurology
74d
Cleared
Aug 01, 2003
MICRUS MICROCOIL SYSTEMS, MODELS HEL, SPH, STR, FSR AND HSR
Neurology
73d
Cleared
Oct 22, 2002
MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01
Neurology
90d
Cleared
Jan 11, 2001
MICRUS MICROCOIL DELIVERY SYSTEM, MDS03
Neurology
189d