Device Classification Name |
Device, Neurovascular Embolization
|
510(k) Number |
K072173 |
Device Name |
MICRUS MICROCOIL SYSTEM CASHMERE-CERECYTE, MODEL CRC; CASHMERE-SR, MODEL SRC |
Applicant |
MICRUS ENDOVASCULAR CORPORATION |
821 FOX LANE |
SAN JOSE,
CA
95131
|
|
Applicant Contact |
PATRICK LEE |
Correspondent |
MICRUS ENDOVASCULAR CORPORATION |
821 FOX LANE |
SAN JOSE,
CA
95131
|
|
Correspondent Contact |
PATRICK LEE |
Regulation Number | 882.5950
|
Classification Product Code |
|
Date Received | 08/06/2007 |
Decision Date | 10/05/2007 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Neurology
|
510k Review Panel |
Neurology
|
Summary |
Summary
|
Type |
Special
|
Reviewed by Third Party |
No
|
Combination Product |
No
|
Recalls |
CDRH Recalls
|
|
|