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Model Number 100-9812 |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
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Patient Problems
Complaint, Ill-Defined (2331); No Code Available (3191)
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Event Date 04/19/2019 |
Event Type
Injury
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Event Description
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It was reported that during the implant procedure the clinical patient, (b)(6) study, experienced a life threatening desaturation.The patient was turned and intubated.The physician decided not to proceed with the l4-5 placement of the device.The patient was successfully implanted at the l3-4 region and is satisfied with the results and has had no complications.
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Event Description
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It was reported that during the implant procedure the clinical patient, a4086 press study, experienced a life threatening desaturation.The patient was turned and intubated.The physician decided not to proceed with the l4-5 placement of the device.The patient was successfully implanted at the l3-4 region and is satisfied with the results and has had no complications.
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Search Alerts/Recalls
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