MAUDE Adverse Event Report: NEVRO CORP. SENZA; NEVRO SENZA

Model Number LEAD3005-70B

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Neurological Deficit/Dysfunction (1982)

Event Date 10/05/2020

Event Type  Injury  

Manufacturer Narrative

The manufacturing records were reviewed and no issues were found related to the nature of the complaint.The device was not returned.

Event Description

It was reported to nevro that during the implant procedure, the patient lost bilateral lower extremity motor function.The physician aborted the case and the patient regained left lower extremity motor function.The patient was transferred to a hospital.The patient¿s motor functions are improving and they¿re going to be discharged to a rehabilitation facility.

• Brand Name: SENZA
• Type of Device: NEVRO SENZA
• Manufacturer (Section D): NEVRO CORP.; 1800 bridge parkway; redwood city CA 94065
• Manufacturer Contact: catherine aronson ; 1800 bridge parkway; redwood city, CA 94065 ; 6504333218
• MDR Report Key: 10923618
• MDR Text Key: 218953418
• Report Number: 3008514029-2020-00806
• Device Sequence Number: 1
• Product Code: LGW
• UDI-Device Identifier: 00813426020480
• UDI-Public: 00813426020480
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: P130022
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 11/30/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/30/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 06/30/2023
• Device Model Number: LEAD3005-70B
• Device Catalogue Number: LEAD3005-70B
• Device Lot Number: 94476482
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 11/07/2020
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 07/02/2020
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Other