FDA Adverse Event Malfunction Summary report: N

MUST MINI STD CROSS CONNECTOR 37MM - STERILE

MDR report key: 8959261 · Received September 4, 2019

Report

Report Number
3005180920-2019-00727
Event Type
Malfunction
Date Received
September 4, 2019
Date of Event
August 5, 2019
Report Date
September 4, 2019
Manufacturer
MEDACTA INTERNATIONAL SA
Product Code
NKG
UDI-DI
07630040706674
PMA / PMN Number
K171369
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 1

BATCH REVIEW PERFORMED ON 8 AUGUST 2019: LOT 1822330: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 5-NOV-2018. EXPIRATION DATE: 2023-10-22. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN ALREADY SOLD WITHOUT ANY SIMILAR REPORTED EVENT. VISUAL INSPECTION PERFORMED BY R&D PROJECT MANAGER: BASED ON THE EVENT DESCRIPTION, IT WAS REALIZED THAT IT WAS RATHER DIFFICULT TO POSITION THE CROSS-CONNECTOR DUE TO OVERALL IMPLANT DESIGN AS WELL AS THE PATIENT ANATOMY. THE INFORMATION GIVEN ON THE IMPLANT IS THE REAL ROD-TO-ROD DISTANCE. HOWEVER, DURING THE SELECTION OF CROSS-CONNECTOR SIZE, IT HAS TO BE CONSIDERED THE MINIMAL DISTANCE BETWEEN THE LIPS OF THE CLAMPS WHEN SEATED IN FULL OPEN POSITION. IN ORDER TO GIVE THE BEST SUPPORT TO THE USERS FOR SIZE SELECTION, A MARKET COMMUNICATION WILL BE ADDRESSED TO ADDITIONALLY DETAIL THE PROPER TECHNIQUE. AT THE END OF THE SURGERY, THE USER PREFERRED NOT TO IMPLANT THE CROSS-CONNECTOR BECAUSE OF ADDITIONAL BONE REMOVAL WAS NECESSARY. SO, IT IS SUPPOSED THAT THERE WERE NO SAFETY RELATED CONCERN THAT MIGHT NEGATIVELY AFFECT THE PATIENT DUE TO NOT POSITIONING THE CROSS-CONNECTOR. THE IMPLANT IS FEATURES WITH A FRICTION INTERFACE TO PREVENT LOOSING AND SLIDING OF THE CLAMP FROM THE TRANSVERSAL BAR, WHICH MAKES THE CLAMP MORE STABLE OVER THE TRANSVERSAL BAR. THE OVERALL DIMENSION OF THE CLAMP SHOULD BE WELL CONSIDERED IN RELATION TO PATIENT ANATOMY AS WELL AS THE DISTANCE BETWEEN THE ADJACENT SCREW-HEAD, IN ORDER TO ALLOW THE CROSS-CONNECTOR POSITIONING. DURING VISUAL INSPECTION IT WAS OBSERVED THAT ALL THE LOCKING SCREWS WERE FULLY ENGAGED IN THE CLAMPS, REDUCING THE CLEARANCE NECESSARY TO POSITION THE CLAMP OVER THE POLY-AXIAL SCREWS-RODS CONSTRUCT. IN CASE OF EXCESSIVE ENGAGEMENT, THE USER HAS TO RELEASE THE LOCKING SCREW IN ORDER TO EASE THE POSITION. THE LOCKING SCREW CAN BE FURTHER DISENGAGED FROM THE CLAMP WITH THE TEMPORARY SET-SCREWDRIVER INCLUDED IN THE INSTRUMENT SET. VISUAL INSPECTION AND FUNCTIONAL CHECKING CONFIRMED THAT THE IMPLANT COMPLIES WITH THE TECHNICAL SPECIFICATION AND IT WAS FUNCTIONAL FOR THE INTENDED USE. ADDITIONAL IMPLANT INVOLVED IN THE EVENT, BATCH REVIEW PERFORMED ON 8 AUGUST 2019 MUST MINI 03.75.716 MUST MINI STD CROSS CONNECTOR 44MM - STERILE (K171369) LOT. 1822331. LOT 1822331: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 5-NOV-2018. EXPIRATION DATE: 2023-10-22. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN ALREADY SOLD WITHOUT ANY SIMILAR REPORTED EVENT.

Description of Event or Problem · 1

STD CROSS CONNECTOR LENGTH 37MM: ALTHOUGH THE MEASURED VALUE OF ROD DISTANCE WAS 37MM, IT WAS NOT ABLE TO SET. STD CROSS CONNECTOR LENGTH 44MM: ALTHOUGH THERE WAS NO PROBLEM FOR THE SIZE OF STD CROSS CONNECTOR LENGTH 44MM, THE CONNECTION PART WITH ROD DID NOT MOVE SMOOTHLY. MOREOVER THE CONNECTION PART WITH ROD WAS THICK, SO IN ORDER TO USE IT THE SURGEON NEEDED TO REMOVE THE BONE ADDITIONALLY. THEREFORE THE SURGEON WAS NOT ABLE TO USE IT FOR THE SURGERY. THE SURGEON FINISHED THE SURGERY WITHOUT USING THE STD CROSS CONNECTOR. DUE TO THIS EVENT THE SURGERY WAS PROLONGED ABOUT 20 MINUTES. IT WAS HARD TO USE IT BECAUSE THE CONNECTION PART WITH ROD DID NOT MOVE SMOOTHLY AND IT WAS THICK. IT DID NOT MAKE SENSE TO USE IT IN CASE ADDITIONALLY BONE REMOVE IS REQUIRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
757099 MUST MINI STD CROSS CONNECTOR 37MM - STERILE CROSS CONNECTOR NKG MEDACTA INTERNATIONAL SA 1822330 07630040706674

Patients

Seq Age Sex Outcome Treatment
1 Other