FDA 510(k) Application Details - K070134

Device Classification Name	Stimulator, Nerve, Battery-Powered   More FDA Info for this Device
510(K) Number	K070134
Device Name	Stimulator, Nerve, Battery-Powered
Applicant	STOCKERT GMBH BOETZINGER STRASSE 72 FREIBURG, B-W D-79111 DE Other 510(k) Applications for this Company
Contact	DOMINIKA SCHULER Other 510(k) Applications for this Contact
Regulation Number	868.2775   More FDA Info for this Regulation Number
Classification Product Code	BXN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/16/2007
Decision Date	03/22/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review