International safety notice
Caja hueca intervertebral Tritanium PL Ver referencias afectadas en la nota de aviso de la empresa ( Apéndice A)
Spain / AEMPS · ESP · Jan 15, 2019
Key facts
| Title | Caja hueca intervertebral Tritanium PL Ver referencias afectadas en la nota de aviso de la empresa ( Apéndice A ) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Caja hueca intervertebral Tritanium PL Ver referencias afectadas en la nota de aviso de la empresa ( Apéndice A ) |
| Manufacturer | Stryker Spine, EEUU. |
| Models | 48953122, 48950130, 48951132, 48953112, 48951080, 48954076, 48951092, 48950146, 48953080, 48951126, 48950116, 48955086 and 105 more |
| Event type | Safety Notice |
| Date | Jan 15, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1