Plate, Cranioplasty, Preformed, Non-Alterable
FDA product code GXN · Class 2 · 112 devices · 232 reports · 0 devices named in recalls
- NA SD800.402Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.429Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.444Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.501Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.510Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.528Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.533Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.534Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD800.535Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD420.526Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD420.427Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report
- NA SD420.433Synthes GmbH · PLATE, CRANIOPLASTY, PREFORMED, NON-ALTERABLE1 report