MAUDE Adverse Event Report: MEDTRONIC NAVIGATION, INC FUSION; INSTRUMENT, STEREOTAXIC

Model Number	9733533
Medical Device Problem Code	Material Integrity Problem (2978)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	02/20/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Patient information was unavailable from the site.No parts have been received by the manufacturer for evaluation.If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
Medtronic received information regarding a navigation system being used in a functional endoscopic sinus surgery (fess).It was reported that there was tracking issue with one of the instruments.So the site used a different and no issue were found with the use of another tracker.
Additional Manufacturer Narrative
The tracker was returned to the manufacturer for evaluation.After functional testing and visual/physical examination the reported issue could not be confirmed.When the tracker was connected to a known good system the tracker was recognized without issue.No problems were found.If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
Medtronic received information regarding a navigation system being used in a functional endoscopic sinus surgery (fess).It was reported that there was tracking issue with one of the instruments.So the site used a different and no issue were found with the use of another tracker.

• Brand Name: FUSION
• Common Device Name: INSTRUMENT, STEREOTAXIC
• Manufacturer (Section D): MEDTRONIC NAVIGATION, INC; 826 coal creek circle; louisville CO 80027
• MDR Report Key: 8417551
• Report Number: 1723170-2019-01091
• Device Sequence Number: 1515549
• Product Code: HAW
• UDI-Device Identifier: 00763000235079
• UDI-Public: 00763000235079
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K001284
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/04/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 9733533
• Device Catalogue Number: 9733533
• Device Lot Number: 180809
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/04/2019
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/20/2019
• Supplement Date Received by Manufacturer: 03/21/2019
• Initial Report FDA Received Date: 03/13/2019
• Supplement Report FDA Received Date: 04/04/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1