Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Wiltrom Corporation Limited

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories2
Latest FDA decision2020-10-23
TypeNumberDevice NameCodeDateActions
510(k) K202894 Wiltrom Spinal Fixation SystemNKB2020-10-23 View
510(k) K180758 Osteocera Resorbable Bone SubstituteMQV2018-10-24 View
510(k) K172237 Bicera Resorbable Bone SubstituteMQV2018-02-02 View
510(k) K172548 Wiltrom Spinal Fixation SystemNKB2018-01-12 View