MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE

Device Classification Name

device, neurovascular embolization

510(k) Number K033813
Device Name MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE
Applicant
MICRUS CORP.
610 palomar avenue
sunnyvale, 
CA 
94085

Applicant Contact margaret webber
Correspondent
MICRUS CORP.
610 palomar avenue
sunnyvale, 
CA 
94085

Correspodent Contact margaret webber
Regulation Number 882.5950
Classification Product Code
HCG  
Date Received 12/09/2003
Decision Date 02/04/2004
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No