FDA 510(k) Application Details - K991002

Device Classification Name	Clip, Implantable   More FDA Info for this Device
510(K) Number	K991002
Device Name	Clip, Implantable
Applicant	V. MUELLER NEURO/SPINE 360 INDUSTRIAL RD., UNIT H SAN CARLOS, CA 94070 US Other 510(k) Applications for this Company
Contact	TERRY JOHNSTON Other 510(k) Applications for this Contact
Regulation Number	878.4300   More FDA Info for this Regulation Number
Classification Product Code	FZP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/25/1999
Decision Date	06/11/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review