MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 6.5MM CANNULATED SCREW 16MM THREAD 100MM; SCREW, FIXATION, BONE

Model Number	208.415
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Pain (1994)
Type of Reportable Event	Serious Injury
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.If the information is unknown, not available or does not apply, the section/field of the form is left blank.Additional narrative: complainant part is not expected to be returned for manufacturer review/investigation.Initial reporter: patient.Without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as 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.
Event or Problem Description
On (b)(6) 2017 patient had a fracture and had undergone pinning percutaneous hip.On (b)(6) 2018 operative reported that the patient was revised due to chronic hip pain right, had removal of screws also and had undergone a total hip arthroplasty left (zimmer/biomet device with omni life femoral stem).6.5mm cannulated screw 16mm thread 80mm (part #208.411 , lot # unknown, quantity# 1).6.5mm cannulated screw 16mm thread 90mm (part # 208.413 , lot # unknown, quantity# 1).6.5mm cannulated screw 16mm thread 105mm (part #208.416, lot # unknown, quantity# 1).6.5mm cannulated screw 16mm thread 100mm (part #208.415, lot # unknown, quantity# 1).This report is for one (16.5mm 6.5mm cannulated screw 16mm thread 100mm.This is report 4 of 4 for complaint (b)(4).

• Brand Name: 6.5MM CANNULATED SCREW 16MM THREAD 100MM
• Common Device Name: SCREW, FIXATION, BONE
• Manufacturer (Section D): WRIGHTS LANE SYNTHES USA PRODUCTS LLC; 1302 wrights lane east; west chester PA 19380
• Manufacturer (Section G): MONUMENT; 1101 synthes avenue; monument CO
• Manufacturer Contact: kate karberg ; 1302 wright lane east; west chester, PA 19380 ; 3035526892
• MDR Report Key: 15364739
• Report Number: 2939274-2022-03412
• Device Sequence Number: 7021056
• Product Code: HWC
• UDI-Device Identifier: 10886982149220
• UDI-Public: (01)10886982149220
• Combination Product (Y/N): N
• Initial Reporter State: NV
• Initial Reporter Country: US
• PMA/510(K) Number: K161616
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2018
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Other
• Type of Report: Initial

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 208.415
• Device Catalogue Number: 208.415
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 08/11/2022
• Initial Report FDA Received Date: 09/06/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 6.5MM CANNULATED SCREW 16MM THREAD 105MM; 6.5MM CANNULATED SCREW 16MM THREAD 80MM; 6.5MM CANNULATED SCREW 16MM THREAD 90MM
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 79 YR
• Patient Sex: Female