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Stryker Ireland Ltd., Instruments Division

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Known Names

stryker ireland ltd., instruments division, stryker ireland, ltd., instruments division

Recent 510(k) Clearances

K-NumberDeviceDate
K082010STRYKER DISPOSABLE CRANIAL PERFORATOR BITDecember 29, 2008
K073633STRYKER ESSX MICRODEBRIDER SYSTEMAugust 26, 2008