FDA 510(k) Application Details - K000021

Device Classification Name	Wax,Bone   More FDA Info for this Device
510(K) Number	K000021
Device Name	Wax,Bone
Applicant	AESCULAP, INC. 13221 MARICOTTE PLACE SAN DIEGO, CA 92130 US Other 510(k) Applications for this Company
Contact	STEVE REITZLER Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	MTJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/04/2000
Decision Date	03/24/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review