NAVLOCK
Report
- Report Number
- 1723170-2025-03385
- Event Type
- Malfunction
- Date Received
- October 3, 2025
- Date of Event
- July 30, 2025
- Report Date
- October 3, 2025
- Manufacturer
- MEDTRONIC NAVIGATION, INC.
- Product Code
- OLO
- PMA / PMN Number
- K124004
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
H3, H6) THE 9734680 (LOT: 180719) PROBE WAS RETURNED TO THE MANUFACTURER FOR EVALUATION. IT WAS FOUND THAT THE TIP OF THE PROBE WAS TWISTED. THE PROBE INSERTED, ROTATED, AND RELEASED FROM A KNOWN GOOD NAVLOCK TRACKER WITHOUT ISSUE. CODES B01, C07, AND D02 ARE APPLICABLE. MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.
MEDTRONIC RECEIVED INFORMATION REGARDING A NAVIGATION SYSTEM BEING USED OUTSIDE OF A PROCEDURE. IT WAS REPORTED THAT THE PROBE WAS D EFORMED. THERE WAS NO PATIENT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1588384 | NAVLOCK | ORTHOPEDIC STEREOTAXIC INSTRUMENT | OLO | MEDTRONIC NAVIGATION, INC. | 9734680 | 180719 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |