Sapphire Medical Group

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K232619MATRIX HA PEEK Cervical IBF SystemMarch 19, 2024
K192316Matrix HA PEEK Cervical Implant SystemOctober 17, 2019
K183073SMG Anterior Cervical Plate SystemFebruary 11, 2019
K172674Sapphire Cervical Implant SystemNovember 2, 2017
K121693A-WEDGE ANTERIOR INTERBODY SYSTEM (A-WEDGE AIS)December 27, 2012