FDA 510(k) Application Details - K992242

Device Classification Name	Prosthesis, Nose, Internal   More FDA Info for this Device
510(K) Number	K992242
Device Name	Prosthesis, Nose, Internal
Applicant	PILLAR SURGICAL, INC. P.O. BOX 8141 LA JOLLA, CA 92038 US Other 510(k) Applications for this Company
Contact	RPB FRITZENKOTTER Other 510(k) Applications for this Contact
Regulation Number	878.3680   More FDA Info for this Regulation Number
Classification Product Code	FZE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/02/1999
Decision Date	11/22/1999
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