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3 records match for Stryker
20181 registryClear
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Not graded by the source2018-08-15FDA MAUDEMW5082031Mako 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 NOTICED A FEMUR DURING PRIMARY TKA.
cause not establishedMW5082031StrykerRead the record ↗Not graded by the source2018-06-26FDA MAUDE0002249697-2018-02287Mako 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 RIGHT MEDIAL KNEE WAS REVISED TO A PS TOTAL KNEE DUE TO PAIN AND OSTEOARTHRITIS.
cause not established0002249697-2018-02287StrykerRead the record ↗Not graded by the source2018-01-24FDA MAUDE3005985723-2018-00081Mako 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: PATIENT HAD A MAKO UNI AND PATELLA FEMORAL REPLACEMENT ON (B)(6) 2017 AND RECENTLY PRESENTED WITH PERSISTENT PAIN. DOCTOR REMOVED IMPLANTS AND REVISED WITH A TOTAL KNEE.
cause not established3005985723-2018-00081StrykerRead the record ↗