FDA 510(k) Applications Submitted by WILTROM CORPORATION LIMITED

FDA 510(k) Number	Submission Date	Device Name	Applicant
K202894	09/28/2020	Wiltrom Spinal Fixation System	Wiltrom Corporation Limited
K180758	03/22/2018	Osteocera Resorbable Bone Substitute	Wiltrom Corporation Limited
K172237	07/25/2017	Bicera Resorbable Bone Substitute	Wiltrom Corporation Limited
K172548	08/23/2017	Wiltrom Spinal Fixation System	Wiltrom Corporation Limited
K110949	04/04/2011	BICERA (TM) RESORBABLE BONE SUBSTITUTE	WILTROM CORPORATION LIMITED