Plate, fixation, bone
FDA product code HRS · Class 2 · 2,808 devices · 6,382 reports · 2 deaths reported · 299 devices named in recalls
- PROFYLE 59-23012Stryker GmbH · PLATE, FIXATION, BONE1 report
- PROFYLE 59-23013Stryker GmbH · PLATE, FIXATION, BONE1 report
- PROFYLE 59-23014Stryker GmbH · PLATE, FIXATION, BONE1 report
- PROFYLE 59-23022Stryker GmbH · PLATE, FIXATION, BONE1 report
- SmartLock 52-27316Stryker GmbH · PLATE, FIXATION, BONE1 report
- VariAx 52-23620Stryker GmbH · PLATE, FIXATION, BONE1 report
- VariAx 58-12010Stryker GmbH · PLATE, FIXATION, BONE1 report
- NA 390157Stryker GmbH · PLATE, FIXATION, BONE1 report