MAUDE Adverse Event Report: SYNTHES GMBH 13 TI CANN RETRO/ANTEGRADE FEM NL/420-S; ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Model Number	04.013.764S
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.Additional narrative: d2b: additional product code: hwc.D9: complainant part is not expected to be returned for manufacturer review/investigation.H3, h6: the investigation could not be completed; no conclusion could be drawn, as no product was received.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) 2022, the patient underwent hardware removal deep due to right femur painful hardware.The plate screws and stimulator bodies were removed.The stimulator electrodes were encased in bone and were not extracted.This report is for one (1) 13 ti cann retro/antegrade fem nl/420-s.This is report 1 of 12 for complaint (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.If the information is unknown, not available or does not apply, the section/field of the form is left blank.Review of the device history record(s) showed that there were no issues during the manufacture of this product, and any sub-components, which would contribute to this complaint condition.Part # 04.013.764s.Synthes lot # 7970944.Supplier lot # n/a.Release to warehouse date: 09 apr 2015.Manufactured by: synthes monument.No ncrs were generated during production.Product was not returned.Based on the information available, it has been determined that no corrective and 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.If information is obtained that was not available for this medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: 13 TI CANN RETRO/ANTEGRADE FEM NL/420-S
• Common Device Name: ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): SYNTHES MONUMENT; 1101 synthes ave; monument CO
• Manufacturer Contact: kate karberg ; 1302 wright lane east; west chester, PA 19380 ; 3035526892
• MDR Report Key: 16709582
• Report Number: 8030965-2023-04392
• Device Sequence Number: 20669171
• Product Code: HSB
• UDI-Device Identifier: 10886982088413
• UDI-Public: (01)10886982088413
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K033618
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup

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: 04.013.764S
• Device Catalogue Number: 04.013.764S
• Device Lot Number: 7970944
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 03/22/2023
• Supplement Date Received by Manufacturer: 04/25/2023
• Initial Report FDA Received Date: 04/10/2023
• Supplement Report FDA Received Date: 05/10/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 04/09/2015
• 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: 4.5 TI VA-LCP CRVD COND PL/12H/266/RT-S; 5.0 LCKNG SCREW SLF-TPNG T25 SD REC 18; 5.0 PERIPR VAL SCR/18 OPTILINK/SF-TPG/SD; 5.0 PERIPR VAL SCR/18 OPTILINK/SF-TPG/SD; 5.0 TI LCKNG SCR T25 SD 34 FOR IM NAILS; 5.0 TI LCKNG SCR T25 SD 66 FOR IM NAILS; 5.0 TI LCKNG SCR T25 SD 76 FOR IM NAILS; 5.0 TI LCKNG SCR T25 SD 76 FOR IM NAILS; 5.0 VAL SCREOPTILINK(TM) SLF-TPNG/SD/20; 5.0 VAL SCREOPTILINK(TM) SLF-TPNG/SD/22; 5.0 VAL SCREOPTILINK(TM) SLF-TPNG/SD/75; 5.0 VAL SCREOPTILINK(TM) SLF-TPNG/SD/80; 5.0 VAL SCREOPTILINK(TM) SLF-TPNG/SD/80
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 63 YR
• Patient Sex: Female