MAUDE Adverse Event Report: ONKOS SURGICAL ELEOS RESURFACING FEMUR, RIGHT; PROSTHESIS, KNEE

Model Number	2500R002E
Medical Device Problem Codes	Loss of or Failure to Bond (1068); Detachment Of Device Component (1104); Loss of Osseointegration (2408); Detachment of Device or Device Component (2907)
Health Effect - Clinical Codes	Unspecified Infection (1930); Patient Problem/Medical Problem (2688)
Date of Event	05/17/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
This report is for one of two devices involved in the event, please refer to report 3013450937-2018-00008 for the other.The device history records and sterilization batch release records were reviewed and indicated that all components involved met specification.The operation notes have been requested along with the explanted components.It was relayed that the components whereabouts are unknown and will not be returned.This investigation is currently ongoing and should additional information be obtained the report will be supplemented.
Event or Problem Description
Revision surgery performed on eleos resurfacing hinge knee where it appeared on x-rays that the resurfacing femur and stem extension had dissociated.Upon removal of the components it was discovered that the resurfacing femur had also loosened.
Additional Manufacturer Narrative
This medical device report (mdr) was initiated as part of a retrospective assessment of complaints under onkos surgical capa (b)(4).As part of this assessment, onkos surgical re-evaluated all complaints received to ensure mdrs were filed when required.The results of this retrospective assessment prompted onkos surgical to file this supplement report.This report is for one of two devices involved in the event, please refer to report 3013450937-2018-00008 for the other.The device history records and sterilization batch release records were reviewed and indicated that all components involved met specification.The operation notes have been requested along with the explanted components.It was relayed that the components whereabouts are unknown and will not be returned.From the available information it was determined that the adverse event was not related to the manufacture of the implants or a non-conformance and this complaint has been closed.Should additional information be obtained to further this investigation, the report will be updated.
Event or Problem Description
Revision surgery performed on eleos resurfacing hinge knee where it appeared on x-rays that the resurfacing femur and stem extension had dissociated.Upon removal of the components it was discovered that the resurfacing femur had also loosened.

• Brand Name: ELEOS RESURFACING FEMUR, RIGHT
• Common Device Name: PROSTHESIS, KNEE
• Manufacturer (Section D): ONKOS SURGICAL; 77 east halsey road; parsippany NJ 07054
• MDR Report Key: 7582367
• Report Number: 3013450937-2018-00009
• Device Sequence Number: 2527305
• Product Code: KRO
• UDI-Device Identifier: B2782500R002E0
• UDI-Public: B2782500R002E0
• Combination Product (Y/N): N
• Initial Reporter State: AL
• Initial Reporter Country: US
• PMA/510(K) Number: K161520
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Health Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/13/2018

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 Expiration Date: 09/28/2025
• Device Model Number: 2500R002E
• Device Catalogue Number: 2500R002E
• Device Lot Number: 1727332
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 05/17/2018
• Supplement Date Received by Manufacturer: 05/17/2018
• Initial Report FDA Received Date: 06/08/2018
• Supplement Report FDA Received Date: 09/13/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 63 YR