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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device device, prosthesis alignment
Product CodeIQO
Regulation Number 890.3025
Device Class 1

MDR Year MDR Reports MDR Events
2016 1 1
2020 1 1

Device Problems MDRs with this Device Problem Events in those MDRs
Break 1 1
Mechanical Jam 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Consequences Or Impact To Patient 1 1
No Information 1 1
No Code Available 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Biomet U.K., Ltd. II Aug-17-2012
2 Stryker Howmedica Osteonics Corp. II Aug-26-2009
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