CONTINUUM® KNEE SYSTEM AUGMENTATION PATELLA ¿¿ SIZE: MEDIUM / THICKN Adverse Event — Injury (MDR 3005751028-2020-00057)
CONTINUUM® KNEE SYSTEM AUGMENTATION PATELLA ¿¿ SIZE: MEDIUM / THICKN Adverse Event — Injury (MDR 3005751028-2020-00057) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CONTINUUM® KNEE SYSTEM AUGMENTATION PATELLA ¿¿ SIZE: MEDIUM / THICKN; Generic name: PROSTHESIS, KNEE; Manuf
| Device | CONTINUUM® KNEE SYSTEM AUGMENTATION PATELLA ¿¿ SIZE: MEDIUM / THICKN |
|---|---|
| Generic name | PROSTHESIS, KNEE |
| Manufacturer | ZIMMER TMT |
| Report number | 3005751028-2020-00057 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | CONSUMER, HEALTH PROFESSIONAL |
| Narrative | (B)(4). CONCOMITANT MEDICAL PRODUCT OSS TIBIAL BEARING, CATALOG #: 150410, LOT #: 875680; OSS POLY TIBIAL BUSHING, CATALOG #: 150476, LOT #: 689570; OSS REINFORED YOKE, CATALOG #: 150493, LOT #: 063820; OSS POROUS IM STEM, CATALOG #: 150403, LOT #: 596730; OSS POLY FEMORAL BUSHINGS, CATALOG #: 150477, LOT #: 745350; OSS PROXIMAL TIBIAL, CATALOG #: 150805, LOT #: 161380; OSS POLY LOCK PIN, CATALOG |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →