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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER GMBH LOCKING SCREW VARIAX2 T10, FULL THREAD, 3.5MM / L12MM; SCREW, FIXATION, BONE

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STRYKER GMBH LOCKING SCREW VARIAX2 T10, FULL THREAD, 3.5MM / L12MM; SCREW, FIXATION, BONE Back to Search Results
Model Number 657312
Medical Device Problem Codes Positioning Failure (1158); Material Fragmentation (1261)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 10/23/2020
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
Upon completion of investigation, additional information will be provided in a supplemental report.
 
Event or Problem Description
As reported: "no blocking was possible - chip formation occurred on the implant.Replacement was available.Surgical delay of 15min.Not longer.".
 
Additional Manufacturer Narrative
The reported event could be confirmed based on the damage pattern shown at the locking thread.The returned locking screw was inspected under a microscope.The thread below the screw head which is intended to lock the screw in the plate, shows plastic deformation which could explain the loss of the angular locking ability.The damage pattern suggests high force application during locking attempts.A potential non-conformity report was initiated to address this event.The comprehensive root cause analysis of the potential ncr included a surface and microstructure analysis as well as nano-indent hardness measurement of variax1 and variax2 screw samples by the fraunhofer institute on behalf of stryker.Further internal investigation efforts were focusing on the anodization color difference between variax1 and variax2 screws.Significant differences between the screws which could result in the reported complaints have not been revealed in either fraunhofer or stryker investigations.Excessive in-house handling and bench testing with variax2 screws from various manufacturing batches showed that locking is achieved as intended.The desired increase in torque indicating to the customer that the screw is locking in the plate, can be confirmed.A review of the device history for the reported lot did not indicate any abnormalities.No deviation from the specifications was noted.No indications of material, manufacturing or design related problems were found during the investigation.A review of the labeling did not indicate any abnormalities.Considering the information given and based on the above investigations a root cause of the reported event could not be determined.If any further substantial information is provided, the investigation report will be updated.
 
Event or Problem Description
As reported: "no blocking was possible - chip formation occurred on the implant.Replacement was available.Surgical delay of 15min.Not longer.".
 
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Brand Name
LOCKING SCREW VARIAX2 T10, FULL THREAD, 3.5MM / L12MM
Common Device Name
SCREW, FIXATION, BONE
Manufacturer (Section D)
STRYKER GMBH
bohnackerweg 1
postfach
selzach 2545
SZ  2545
MDR Report Key10891139
Report Number0008031020-2020-02495
Device Sequence Number11536987
Product Code HWC
UDI-Device Identifier07613327086812
UDI-Public07613327086812
Combination Product (Y/N)N
Initial Reporter CountryGM
PMA/510(K) Number
K180500
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source health professional
Initial Reporter Occupation Physician
Type of Report Initial,Followup
Report Date (Section B) 03/23/2021
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 Number657312
Device Catalogue Number657312
Device Lot NumberL50711
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer11/12/2020
Initial Date Received by Manufacturer 10/29/2020
Supplement Date Received by Manufacturer02/25/2021
Initial Report FDA Received Date11/24/2020
Supplement Report FDA Received Date03/23/2021
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
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