FDA Adverse Event Injury Summary report: N

MEDTRONIC NAVIGATION

MDR report key: 9272786 · Received November 4, 2019

Report

Report Number
1723170-2019-05461
Event Type
Injury
Date Received
November 4, 2019
Date of Event
April 10, 2018
Report Date
November 4, 2019
Manufacturer
MEDTRONIC NAVIGATION, INC
Product Code
HAW
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PATIENT WEIGHT NOT AVAILABLE FROM THE SITE. EVENT DATE IS THE ACCEPTED DATE OF THE ARTICLE FOR PUBLICATION. DEVICE LOT NUMBER, OR SERIAL NUMBER, UNAVAILABLE. NO PARTS HAVE BEEN RECEIVED BY THE MANUFACTURER FOR EVALUATION. DEVICE MANUFACTURING DATE IS DEPENDENT ON LOT NUMBER/SERIAL NUMBER, THEREFORE, UNAVAILABLE. OTHER RELEVANT DEVICE(S) ARE: PRODUCT ID: UNK_OARM_SYS, SERIAL/LOT #: UNK. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

CITATION: MOURAD OULD-SLIMANE, FRANC¸OIS-XAVIER FERRACCI, SÉBASTIEN LE PAPE, ALEXIS PEREZ, PAUL MICHELIN, RÉMI GAUTHÉ. POSTERIOR C1C2 HARMS FUSION WITH 3D SURGICAL NAVIGATION. ORTHOPAEDICS AND TRAUMATOLOGY: SURGERY AND RESEARCH 104(2018) 585-588. ABSTRACT: SEVERAL TYPES OF ATLANTOAXIAL INSTABILITY CAN JUSTIFY SURGICAL FIXATION. THE INSTRUMENTED FUSION PROCEDURE DESCRIBED BY HARMS WITH SCREW FIXATION OF THE C1 LATERAL MASSES AND C2 PEDICLES IS A DEMANDING TECHNIQUE THAT PROVIDES LASTING STABILIZATION. HOWEVER, IT HAS BEEN ASSOCIATED WITH NERVE AND VASCULAR COMPLICATIONS DUE TO THE LOCAL ANATOMICAL CONFIGURATION. SURGICAL NAVIGATION SYSTEMS CAN HELP IMPROVE THE PROCEDURE¿S ACCURACY. WE DESCRIBE A SERIES OF 11 CASES OF C1C2 HARMS FUSION PERFORMED WITH SURGICAL NAVIGATION AND INTRAOPERATIVE 3D IMAGING CHECKS. ALL PROCEDURES WERE CARRIED OUT COMPLETELY WITH SATISFACTORY IMPLANT PLACEMENT. THERE WERE NO ADVERSE EVENTS RELATED TO THE PROCEDURE DURING THE PERI-OPERATIVE PERIOD. NO CORTICAL BREACH WAS DETECTED USING CONE-BEAM CT AT THE END OF THE PROCEDURE. THE TECHNICAL CHALLENGES AND RISKS ASSOCIATED WITH C1C2 HARMS FUSION HAVE LED TO THE USE OF 3D INTRAOPERATIVE IMAGING SYSTEMS, WHEN AVAILABLE. REPORTED EVENTS: ONE PATIENT EXPERIENCED POST-OPERATIVE NECK PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1066341 MEDTRONIC NAVIGATION INSTRUMENT, STEREOTAXIC HAW MEDTRONIC NAVIGATION, INC UNK_NAV_SYS

Patients

Seq Age Sex Outcome Treatment
1 67 YR Required Intervention