FDAMarch 16, 2017device
Altius M-INI OCT Posterior Spinal Fixation System, Model Number 1200-9216 The AltiusTM OCT and AltiusTM M-INITM OCT Systems when intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (Occiput-T3), these systems are indicated for: DDD (neck pain of discogenic origi...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Zimmer Biomet is recalling the Altius M-INI OCT Posterior Spinal Fixation System because the driver is unable to mate with the screw head tulip.
What to do
FDA enforcement status: Terminated
Brands named
zimmer biomet spinezimmerzimmer biomet
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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