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Stryker Ent

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K201398SINUSPRIME Dilation SystemOctober 15, 2020
K193118TGS Guidewire and updated Scopis SoftwareFebruary 21, 2020
K193502TGS Universal Headrest with Mounting ArmFebruary 14, 2020