MAUDE Adverse Event Report: WRIGHTS LANE SYNTHES USA PRODUCTS LLC 5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/85MM; SCREW, FIXATION, BONE

Model Number	02.231.285
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
Complainant part is not expected to be returned for manufacturer review/investigation.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
It was reported that on (b)(6) 2020, the patient underwent a hardware removal due to pain.The screw length of the four (4) variable angle locking screw and one (1) cannulated variable angle locking screw were too long and were causing pain.The screws were replaced with shorter screws.The procedure outcome is unknown.Concomitant device reported: unknown curved condylar plate (part# unknown, lot# unknown, quantity# unknown).This is report 4 of 5 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.H10 additional narrative: d7: updated explantation date.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: 5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/85MM
• 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: 10201214
• Report Number: 2939274-2020-03011
• Device Sequence Number: 16412073
• Product Code: HWC
• UDI-Device Identifier: 10886982062246
• UDI-Public: (01)10886982062246
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• PMA/510(K) Number: K110354
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 06/16/2020

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: 02.231.285
• Device Catalogue Number: 02.231.285
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 06/16/2020
• Supplement Date Received by Manufacturer: 06/29/2020
• Initial Report FDA Received Date: 06/26/2020
• Supplement Report FDA Received Date: 07/15/2020
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 5.0MM CANNULATED VA LOCKING SCREW/90MM.; 5.0MM VA LOCKNG SCREW/85MM.; 5.0MM VA LOCKNG SCREW/90MM.; 5.0MM VA LOCKNG SCREW/90MM.; UNK - PLATES: 4.5MM VA LCP CONDYLAR PLATE.; 5.0MM CANNULATED VA LOCKING SCREW/90MM; 5.0MM VA LOCKNG SCREW/85MM; 5.0MM VA LOCKNG SCREW/90MM; 5.0MM VA LOCKNG SCREW/90MM; UNK - PLATES: 4.5MM VA LCP CONDYLAR PLATE
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 73 YR