MAUDE Adverse Event Report: ONKOS SURGICAL ELEOS; CEMENTED STEM EXTENSION, 12X65MM, STRAIGHT, FLUTED

Model Number	KSC01265E
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	01/12/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The investigation is in process.When the investigation is complete and if additional information is received, a supplemental mdr will be submitted accordingly.The following mdrs were submitted for this event: #3013450937-2022-00055; #3013450937-2022-00056; #3013450937-2022-00057; #3013450937-2022-00058; #3013450937-2022-00059; #3013450937-2022-00060; #3013450937-2022-00062.The following mdrs were also submitted for this patient: #3013450937-2022-00007; #3013450937-2022-00008; #3013450937-2022-00009; #3013450937-2022-00010; #3013450937-2022-00011; #3013450937-2022-00012; #3013450937-2022-00013; #3013450937-2022-00014.
Event or Problem Description
It was reported that the patient underwent a revision surgery on (b)(6) 2022 due to an alleged infection.The surgeon performed a poly swap.The following eleos implants were revised: distal femur axial pin, tibial hinge component, and poly spacer.The following eleos implants remain implanted from the patient's original surgery on (b)(6) 2021: distal femur, cemented segmental stem, male-female midsection, cemented stem extension, and tibial baseplate.Additional information regarding this adverse event has not been provided.
Additional Manufacturer Narrative
This report is being submitted to include additional information.The investigation is complete.The device was not returned for evaluation.The root cause of the alleged infection could not be determined.The device history records and sterilization batch records were reviewed and no issues during manufacturing or sterilization were identified that would have contributed to this complaint.If any additional information is obtained, a supplemental mdr will be filed accordingly.The following sections were updated: b4: date of this report added.G3: date received by manufacturer added.G6: type of report added.H2: follow-up type added.H3: device evaluated by manufacturer updated to no.H6: type of investigation code updated to 3331: analysis of production records.H6: type of investigation code updated to 4111: communication/interviews.H6: type of investigation code updated to 4110: trend analysis.H6: type of investigation code updated to 4114: device not returned.H6: type of investigation code updated to 4117: device not accessible for testing.H6: type of investigation code updated to 4109: historical data analysis.H6: investigation findings code updated to 213: no device problem found.H6: investigation conclusions code updated to 4315: cause not established.H10: additional narratives/data.
Event or Problem Description
It was reported that the patient underwent a revision surgery on (b)(6) 2022 due to an alleged infection.The surgeon performed a poly swap.The following eleos implants were revised: distal femur axial pin, tibial hinge component, and poly spacer.The following eleos implants remain implanted from the patient's original surgery on (b)(6)2021: distal femur, cemented segmental stem, male-female midsection, cemented stem extension, and tibial baseplate.Additional information regarding this adverse event has not been provided.

• Brand Name: ELEOS
• Common Device Name: CEMENTED STEM EXTENSION, 12X65MM, STRAIGHT, FLUTED
• Manufacturer (Section D): ONKOS SURGICAL; 77 east halsey road; parsippany NJ 07054
• Manufacturer (Section G): MICROPORT ORTHOPEDICS; 5677 airline road; arlington TN 38002
• Manufacturer Contact: sara dailey ; 77 east halsey road; parsippany, NJ 07054
• MDR Report Key: 13487341
• Report Number: 3013450937-2022-00061
• Device Sequence Number: 14739294
• Product Code: KRO
• UDI-Device Identifier: B278KSC01265E0
• UDI-Public: B278KSC01265E0
• Combination Product (Y/N): N
• Initial Reporter State: IN
• Initial Reporter Country: US
• PMA/510(K) Number: K161520
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 04/10/2022

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: KSC01265E
• Device Catalogue Number: KSC01265E
• Device Lot Number: 1859500
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/10/2022
• Supplement Date Received by Manufacturer: 04/08/2022
• Initial Report FDA Received Date: 02/08/2022
• Supplement Report FDA Received Date: 04/10/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 09/10/2020
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: P/N 25000009E, ELEOS DISTAL FEMUR.; P/N 25000013E, ELEOS CEMENTED SEGMENTAL STEM.; P/N 25001040E, ELEOS MALE-FEMALE MIDSECTION.; P/N 25001208E, ELEOS TIBIAL POLY SPACER.; P/N 25002111E, ELEOS DISTAL FEMUR AXIAL PIN.; P/N TB-2203E-01M, ELEOS TIBIAL BASEPLATE.; P/N THSMWRS01M, ELEOS TIBIAL HINGE COMPONENT.
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 58 YR
• Patient Sex: Female