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Orthocor Medical

FDA Regulatory Profile

Orthocor Medical appears in FDA public data with 0 recalls, 3 510(k) clearances, 6 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 6, 2013.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
6
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

FDA data resources