Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K082474
Device Classification Name
Electrode, Cortical
More FDA Info for this Device
510(K) Number
K082474
Device Name
Electrode, Cortical
Applicant
PMT CORP.
1500 PARK RD.
CHANHASSEN, MN 55317 US
Other 510(k) Applications for this Company
Contact
ERIC CAILLE
Other 510(k) Applications for this Contact
Regulation Number
882.1310
More FDA Info for this Regulation Number
Classification Product Code
GYC
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
08/28/2008
Decision Date
05/08/2009
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact