FDA 510(k) Application Details - K011567

Device Classification Name	Prosthesis, Elbow, Semi-Constrained, Cemented   More FDA Info for this Device
510(K) Number	K011567
Device Name	Prosthesis, Elbow, Semi-Constrained, Cemented
Applicant	TORNIER ZIRST-161, RUE LAVOISIER MONTBONNOT 38330 FR Other 510(k) Applications for this Company
Contact	IRENE GOSSET Other 510(k) Applications for this Contact
Regulation Number	888.3160   More FDA Info for this Regulation Number
Classification Product Code	JDB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/21/2001
Decision Date	06/19/2001
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