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Osteomed Implantes, Ltda

FDA Regulatory Profile

Osteomed Implantes, Ltda appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Feb 10, 2016.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K151553Anterior Cervical Plate SystemFeb 10, 2016
K143572Intersomatic Cervical Device - DICOM PEEK, Intersomatic Intervertebral Space Maintenance Device - DIJun 10, 2015
K150294DPZ Pedicular Fixation SystemJun 5, 2015

FDA data resources