FDA 510(k) Application Details - K030665

Device Classification Name	Pin, Fixation, Smooth   More FDA Info for this Device
510(K) Number	K030665
Device Name	Pin, Fixation, Smooth
Applicant	STORK INSTRUMENTE GMBH 7046 BENTLY DR. GURNEE, IL 60031 US Other 510(k) Applications for this Company
Contact	LORI ADVIDS Other 510(k) Applications for this Contact
Regulation Number	888.3040   More FDA Info for this Regulation Number
Classification Product Code	HTY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/03/2003
Decision Date	03/25/2003
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