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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
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