Stryker Ireland Ltd., Instruments Division

FDA Regulatory Profile

Stryker Ireland Ltd., Instruments Division appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 29, 2008.

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