MAUDE Adverse Event Report: DEPUY IRELAND - 9616671 ATUN PRESSFIT STR STEM18X110MM; KNEE STEMS

Model Number	1513-18-110
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Bone Fracture(s) (1870)
Date of Event	05/20/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product complaint # (b)(4).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
The patient was revised to address spiral fracture of the femur starting at the proximal tip of the attune press fit fluted stem.Attune knee revision was performed on 5/20.Case went well and surgeon was contact with outcome.Attune revision surgical technique was followed perfectly.No surgical delay.Doi: unknown, dor: (b)(6) 2021, left knee.
Additional Manufacturer Narrative
Product complaint (b)(4).Investigation summary : no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot : the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.
Additional Manufacturer Narrative
Product complaint #: (b)(4).This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information prior to the required reporting date.This report does not reflect a conclusion by depuy synthes joint reconstruction, or its employees that the report constitutes an admission that the product, depuy synthes joint reconstruction, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.

• Brand Name: ATUN PRESSFIT STR STEM18X110MM
• Common Device Name: KNEE STEMS
• Manufacturer (Section D): DEPUY IRELAND - 9616671; loughbeg ringaskiddy co.; cork ; EI
• MDR Report Key: 11992182
• Report Number: 1818910-2021-12537
• Device Sequence Number: 19033815
• Product Code: JWH
• UDI-Device Identifier: 10603295043737
• UDI-Public: 10603295043737
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: P830055
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 05/20/2021

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: 1513-18-110
• Device Catalogue Number: 151318110
• Device Lot Number: JC7877
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 05/20/2021
• Supplement Date Received by Manufacturer: 07/09/2021; 06/25/2021
• Initial Report FDA Received Date: 06/14/2021
• Supplement Report FDA Received Date: 07/12/2021; 07/16/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: ATTUNE CRS FEMORAL LT SZ 5 CEM.; ATTUNE CRS RP INSRT SZ 5 6MM.; ATTUNE MEDIAL DOME PAT 38MM.; ATUN PRESSFIT STR STEM18X110MM.; ATUN TIB SLV M/L 45MM FULL POR.; SMARTSET GHV GENTAMICIN 40G.; ATTUNE CRS FEMORAL LT SZ 5 CEM; ATUN PRESSFIT STR STEM18X110MM
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 62 YR