FDA 510(k) Application Details - K070031

Device Classification Name	Staple, Fixation, Bone   More FDA Info for this Device
510(K) Number	K070031
Device Name	Staple, Fixation, Bone
Applicant	MEMOMETAL TECHNOLOGIES RUE BLAISE PASCAL CAMPUS DE KER LANN BRUZ F35170 FR Other 510(k) Applications for this Company
Contact	GILLES AUDIC Other 510(k) Applications for this Contact
Regulation Number	888.3030   More FDA Info for this Regulation Number
Classification Product Code	JDR Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/03/2007
Decision Date	03/19/2007
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