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Not graded by the source2015-10-22FDA MAUDE3005985723-2015-00245Mako Robotic-Arm
Mako Robotic-Arm — Injury report filed with FDA (MAUDE). A MAUDE report does not establish that the device caused the outcome. Reported narrative: SURGEON REVISED LEFT MAKO KNEE DUE TO PAIN AND INFECTION.
cause not established3005985723-2015-00245StrykerRead the record ↗