FDA 510(k) Application Details - K954757

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K954757
Device Name	Screw, Fixation, Bone
Applicant	FERGUSON MEDICAL 3407 BAY AVE. CHICO, CA 95973-8619 US Other 510(k) Applications for this Company
Contact	FRANK FERGUSON Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	HWC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/16/1995
Decision Date	01/25/1996
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