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NEXGEN® COMPLETE KNEE SOLUTION, TRABECULAR METAL¿¢ STANDARD PRIMARY Adverse Event — Injury (MDR 3005751028-2020-00036)

NEXGEN® COMPLETE KNEE SOLUTION, TRABECULAR METAL¿¢ STANDARD PRIMARY Adverse Event — Injury (MDR 3005751028-2020-00036) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NEXGEN® COMPLETE KNEE SOLUTION, TRABECULAR METAL¿¢ STANDARD PRIMARY; Generic name: PROSTHESIS, KNEE; Manufac

DeviceNEXGEN® COMPLETE KNEE SOLUTION, TRABECULAR METAL¿¢ STANDARD PRIMARY
Generic namePROSTHESIS, KNEE
ManufacturerZIMMER TMT
Report number3005751028-2020-00036
Event typeInjury
Product problemN
Date received2020-04-27
Report sourceHEALTH PROFESSIONAL, STUDY
Narrative(B)(4). CONCOMITANT MEDICAL PRODUCT: PERSONA FEMUR (PS) CATALOG 42500806601 LOT 62718131 LOT 62718131; PERSONA NATURAL TIBIA CATALOG 42530007101 LOT 62584836; PERSONA ARTICULAR SURFACE CATALOG 42511400710 LOT 62779854. MEDICAL RECORDS PROVIDED SHOWED PATIENT REPORTED PAIN AND NO DIFFICULTY WITH MOBILITY AT THE 1-YEAR FOLLOW-UP AND CONTINUED PAIN AT THE 2-YEAR FOLLOW-UP. THERE HAS BEEN NO MEDICAL I
SourceopenFDA MAUDE (device adverse events)

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