FDA 510(k) Application Details - K102488

Device Classification Name	Orthosis, Spondyloisthesis Spinal Fixation   More FDA Info for this Device
510(K) Number	K102488
Device Name	Orthosis, Spondyloisthesis Spinal Fixation
Applicant	SPINECRAFT LLC 2215 ENTERPRISE DRIVE SUITE 1504 WESTCHESTER, IL 60154 US Other 510(k) Applications for this Company
Contact	AMI AKALLAL-ASAAD Other 510(k) Applications for this Contact
Regulation Number	888.3070   More FDA Info for this Regulation Number
Classification Product Code	MNH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/31/2010
Decision Date	12/10/2010
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