FDA 510(k) Application Details - K973586

Device Classification Name	Screw, Fixation, Bone   More FDA Info for this Device
510(K) Number	K973586
Device Name	Screw, Fixation, Bone
Applicant	SPINAL CONCEPTS, INC. 820O CAMERON RD., SUITE B-160 AUSTIN, TX 78754 US Other 510(k) Applications for this Company
Contact	TEENA M AUGOSTINO 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	09/22/1997
Decision Date	11/07/1997
Decision	SN - Substantially Equivalent for Some Indications
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status
Type	Traditional
Reviewed By Third Party	N
Expedited Review