Osteomed Implantes, Ltda

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K151553Anterior Cervical Plate SystemFebruary 10, 2016
K143572Intersomatic Cervical Device - DICOM PEEK, Intersomatic Intervertebral Space Maintenance Device - DIJune 10, 2015
K150294DPZ Pedicular Fixation SystemJune 5, 2015