FDA 510(k) Application Details - K101939

Device Classification Name	Rod, Fixation, Intramedullary And Accessories   More FDA Info for this Device
510(K) Number	K101939
Device Name	Rod, Fixation, Intramedullary And Accessories
Applicant	MERETE MEDICAL GMBH 49 PURCHASE STREET RYE, NY 10580 US Other 510(k) Applications for this Company
Contact	DONNA COLEMAN Other 510(k) Applications for this Contact
Regulation Number	888.3020   More FDA Info for this Regulation Number
Classification Product Code	HSB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/12/2010
Decision Date	10/07/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review