Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K030674
Device Classification Name
Stimulator, Spinal-Cord, Implanted (Pain Relief)
More FDA Info for this Device
510(K) Number
K030674
Device Name
Stimulator, Spinal-Cord, Implanted (Pain Relief)
Applicant
ADVANCED NEUROMODULATION SYSTEMS
6501 WINDCREST DRIVE SUITE 100
PLANO, TX 75024 US
Other 510(k) Applications for this Company
Contact
DREW JOHNSON
Other 510(k) Applications for this Contact
Regulation Number
882.5880
More FDA Info for this Regulation Number
Classification Product Code
GZB
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
03/04/2003
Decision Date
03/28/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
NE - Neurology
Review Advisory Committee
NE - Neurology
Statement / Summary / Purged Status
Statement
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact