FDA 510(k) Application Details - K110783

Device Classification Name	Intervertebral Fusion Device With Bone Graft, Lumbar   More FDA Info for this Device
510(K) Number	K110783
Device Name	Intervertebral Fusion Device With Bone Graft, Lumbar
Applicant	L & K BIOMED CO., LTD ROOM 1104, ACE HIGH-END TOWER3 371-50 GASAN-DONG, GEUMCHEON-G SEOUL 153803 KR Other 510(k) Applications for this Company
Contact	HEE KYEONG JOO Other 510(k) Applications for this Contact
Regulation Number	888.3080   More FDA Info for this Regulation Number
Classification Product Code	MAX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/21/2011
Decision Date	10/24/2011
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