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2 records match for Stryker
20171 registryClear
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Not graded by the source2017-12-05FDA MAUDE0002249697-2017-03778Mako 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: IT WAS REPORTED THAT PATIENT'S LEFT MAKO UNICOMPARTMENTAL KNEE WAS REVISED DUE TO MCL INSTABILITY.
cause not established0002249697-2017-03778StrykerRead the record ↗Not graded by the source2017-04-04FDA MAUDE0002249697-2017-01416Mako 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 DID AN I&D WITH AN INSERT SWAP OF THE LEFT KNEE DONE AS A MAKO MEDIAL ORIGINALLY ON (B)(6) 2017.
cause not established0002249697-2017-01416StrykerRead the record ↗