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Orthocor Medical

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K121702ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICEMay 6, 2013
K092044ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGEDecember 18, 2009
K091996ORTHOCOR KNEE SYSTEM BASICDecember 15, 2009