MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 2.4MM CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 18MM; SCREW, FIXATION, BONE

Model Number	201.768
Medical Device Problem Codes	Fitting Problem (2183); Device-Device Incompatibility (2919); Device Difficult to Maintain (3134)
Health Effect - Clinical Code	No Patient Involvement (2645)
Date of Event	04/05/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional pro-code hrs.Complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received.Without a lot number, the device history records review could not be completed as no product was received.The investigation could not be completed; no conclusion could be drawn at the time of filing this report.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
It was reported that on (b)(6) 2019, a 3 hole shaft variable angle locking compression plate (va-lcp) distal radius two column 6hh narrow was used.The surgeon attempted to insert one (1) cortex screw self-tapping with t8 stardrive recess 18mm through the 6 hole guiding block.The screw would not fit through the guide.Other screws were tried.Two (2) additional cortex screw self-tapping with t8 stardrive recess 18mm would not fit through the guide and finally one did.There was a 5 minutes surgical delay.Procedure was successfully completed.The patient was not affected.Concomitant device reported: 3 hole shaft variable angle locking compression plate (va-lcp) (part #unknown, lot # unknown, quantity # 1).This complaint involves four (4) devices.This report if for one (1) 2.4mm cortex screw slf-tpng with t8 stardrive recess 18mm.This report is 1 of 4 for (b)(4).
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.Visual inspection: the screws were visually inspected.Light surface wear, consistent with use and which would not impact the functionality, was noted.No defects were identified on either screw.Functional test: functional test was performed via returned mating device.It was confirmed that all the screws and all the mating grooves of guide block were not fitting.The condition was determined to agree with the complaint description as the cortex screw and mating guide are not intended to fit.Document/specification review: document/specification review the following drawings for the complaint were reviewed: 2.4mm cortex screw, t8 stardrive, 4mm head; cortex screw d2.4xl.The following drawings for the mating device were reviewed: guide block for va-lcp, tcp, 6 holes, left; guide block body (component); set screw for guide block body.Dimensional analysis: the variable angle lcp two -column volar distal radius plate 2.4 technique guide and the 2.4mm variable angle lcp distal radius system technique guide were reviewed and it was confirmed that cortex screws are not intended to be placed through the guide block.Therefore, dimensional analysis was not performed for this screw.Based on design investigation, the original complaint and investigation focused on the surgeon attempting to insert a cortex screw through a guide block for two column plate.This section of the two-column plate family that receives the guide block for neutral angle screw placement contains va-lcp holes.These holes do not correlate with the usage of cortex screws.The surgical technique for the us and eu both define the usage of threaded locking head implants with the use of the guide block.The surgeon in this case is using a screw/plate combination that is not indicated for this particular combination and therefore the complaint can be categorized as user error.Based on the investigation findings, it has been determined that no corrective and/or preventative action is proposed.Additional monitoring for any potential safety signals will be conducted through complaint trending and other post market safety surveillance activities.Corrected data: device codes 3134 and 2183 were inadvertently included on the initial report and are not applicable.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Additional Manufacturer Narrative
Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.The device has been received, the investigation is in progress, no conclusion could be drawn at the time of filing this report.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: 2.4MM CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 18MM
• Common Device Name: SCREW, FIXATION, BONE
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• MDR Report Key: 8580051
• Report Number: 2939274-2019-57832
• Device Sequence Number: 2192190
• Product Code: HWC
• UDI-Device Identifier: 10886982142771
• UDI-Public: (01)10886982142771
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• PMA/510(K) Number: K112583
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 04/05/2019

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: 201.768
• Device Catalogue Number: 201.768
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/30/2019
• Initial Date Received by Manufacturer: 04/05/2019
• Supplement Date Received by Manufacturer: 04/30/2019; 05/31/2019
• Initial Report FDA Received Date: 05/03/2019
• Supplement Report FDA Received Date: 05/30/2019; 06/04/2019
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 3 HOLE SHAFT (VA-LCP)