International safety notice
X-spine Systems (Xtent)
United Kingdom / MHRA · GBR · Sep 1, 2018
Key facts
| Title | X-spine Systems (Xtent) |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Calix Lumbar Spinal Implant System |
| Manufacturer | X-spine Systems (Xtent) |
| Models | 19212-7, 039775, 20164-6, 055545, 054541, 18890-520590-10, 19147-6A, 055211, 19742-3, 042050, 059822, M697X0340286PC1 and 303 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Sep 1, 2018 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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