JDR

COMPRESSYN STAPLE

Advisory panel
Orthopedic
Total cleared
231

Adverse events under product code JDR

product code JDR
Injury
726
Malfunction
663
Other
1
Total
1,390

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code JDR

1–100 of 231

Data sourced from openFDA. This site is unofficial and independent of the FDA.