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

Model Number	KPONTP32E
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	11/11/2017
Type of Reportable Event	Serious Injury
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 report.This report is for one of nine devices involved in this event, please refer to report 3013450937-2018-00046, 3013450937-2018-00047, 3013450937-2018-00048, 3013450937-2018-00050, 3013450937-2018-00051, 3013450937-2018-00052, 3013450937-2018-00053, and 3013450937-2018-00054 for the others.The device history records and sterilization batch release records were reviewed and indicated that the components involved met specification.Additionally, operation notes were provided, which indicated that the patient has had a history of infection.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, the complaint will be re-opened, and this report will be supplemented.
Event or Problem Description
Patient underwent a revision surgery, due to an alleged infection, where all eleos components were removed and an antibiotic cement spacer was placed.

• Brand Name: ELEOS RESURFACING PATELLA
• Common Device Name: PROSTHESIS, KNEE
• Manufacturer (Section D): ONKOS SURGICAL; 77 east halsey road; parsippany NJ 07054
• MDR Report Key: 7851210
• Report Number: 3013450937-2018-00049
• Device Sequence Number: 19262202
• Product Code: KRO
• UDI-Device Identifier: B278KPONTP32E0
• UDI-Public: B278KPONTP32E0
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K161520
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 09/06/2018

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: 03/07/2025
• Device Model Number: KPONTP32E
• Device Catalogue Number: KPONTP32E
• Device Lot Number: 1697851
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/12/2017
• Initial Report FDA Received Date: 09/06/2018
• 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: 73 YR