MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2019-01-24 for NUVASIVENVM5 SYSTEM NVM5MULTI manufactured by Nuvasive.
[135371689]
Product was returned and investigation was performed. Latest logs saved were from october and event was reported in december. Edge cards were replaced unrelated to reported event. Power cycled unit 3 times and ran dynamic stim tests without any issues.
Patient Sequence No: 1, Text Type: N, H10
[135371690]
As per reporter device provided inaccurate readings and screw breach was noted during x-ray review. It is unknown if patient underwent a revision procedure or if screw breach was addressed intra-operative.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2031966-2019-00155 |
MDR Report Key | 8276550 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2019-01-24 |
Date of Report | 2019-01-24 |
Date Mfgr Received | 2018-12-03 |
Device Manufacturer Date | 2018-12-03 |
Date Added to Maude | 2019-01-24 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. YOBANA SANCHEZ |
Manufacturer Street | 7475 LUSK BOULEVARD |
Manufacturer City | SAN DIEGO CA 92121 |
Manufacturer Country | US |
Manufacturer Postal | 92121 |
Manufacturer Phone | 8589093383 |
Manufacturer G1 | NUVASIVE |
Manufacturer Street | 7475 LUSK BOULEVARD |
Manufacturer City | SAN DIEGO CA 92121 |
Manufacturer Country | US |
Manufacturer Postal Code | 92121 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NUVASIVENVM5 SYSTEM |
Generic Name | NEUROSURGICAL NERVE LOCATOR |
Product Code | PDQ |
Date Received | 2019-01-24 |
Model Number | NVM5MULTI |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | NUVASIVE |
Manufacturer Address | 7475 LUSK BOULEVARD SAN DIEGO 92121 US 92121 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-01-24 |