FDA 510(k) Application Details - K033927

Device Classification Name	Arthroscope   More FDA Info for this Device
510(K) Number	K033927
Device Name	Arthroscope
Applicant	W.O.M. WORLD OF MEDICINE AG 368 NORTH ASAPH STREET ALEXANDRIA, VA 22314 US Other 510(k) Applications for this Company
Contact	SUSANNE RAAB Other 510(k) Applications for this Contact
Regulation Number	888.1100   More FDA Info for this Regulation Number
Classification Product Code	HRX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/18/2003
Decision Date	01/15/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review