MAUDE Adverse Event Report: ONKOS SURGICAL ELEOS; STEM EXTENSION, CANAL FILLING

Model Number KSP20100E

Device Problems Loose or Intermittent Connection (1371); Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Unspecified Infection (1930); Insufficient Information (4580)

Event Date 01/05/2022

Event Type  Injury  

Manufacturer Narrative

The investigation is in progress.When it is complete a supplemental mdr will be submitted accordingly.Multiple mdrs were submitted for this adverse event: 3013450937-2022-00047, 3013450937-2022-00048, 3013450937-2022-00049, 3013450937-2022-00050, 3013450937-2022-00051, 3013450937-2022-00052 and 3013450937-2022-00053.

Event Description

It was reported that the patient presented with an alleged disassociated stem on the resurfacing femur and an alleged infection on (b)(6) 2022, after receiving a proximal tibia replacement surgery on (b)(6) 2020.The implanting surgeon performed revision surgeries on the patient to wash the patient out on (b)(6) 2022 and (b)(6) 2022.The surgeon also performed a revision surgery on (b)(6) 2022 to remove all the implants that were implanted on (b)(6) 2020 during the original the proximal tibia replacement surgery.It was also reported that the surgeon plans to put in replacement implants when the infection clears up.No revision surgery to do this has been scheduled yet.No additional information regarding this adverse event has been provided.

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 implant loosening could not be determined.If any additional information is obtained, a supplemental mdr will be filed accordingly.The following sections were updated: h3: device evaluated by manufacturer updated to no.H6: type of investigation code updated to 4110: trend analysis.H6: type of investigation code updated to 4117: device not accessible for testing.H6: investigation findings code updated to 3221: no findings available.H6: investigation conclusions code updated to 4315: cause not established.

Event Description

It was reported that the patient presented with an alleged disassociated stem on the resurfacing femur and an alleged infection on (b)(6) 2022, after receiving a proximal tibia replacement surgery on (b)(6) 2020.The implanting surgeon performed revision surgeries on the patient to wash the patient out on (b)(6) 2022.The surgeon also performed a revision surgery on (b)(6) 2022 to remove all the implants that were implanted on (b)(6) 2020 during the original the proximal tibia replacement surgery.It was also reported that the surgeon plans to put in replacement implants when the infection clears up.No revision surgery to do this has been scheduled yet.No additional information regarding this adverse event has been provided.

• Brand Name: ELEOS
• Type of Device: STEM EXTENSION, CANAL FILLING
• 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: danielle pierce ; 77 east halsey road; parsippany 07054 ; 8447672766
• MDR Report Key: 13458682
• MDR Text Key: 287924609
• Report Number: 3013450937-2022-00046
• Device Sequence Number: 1
• Product Code: KRO
• UDI-Device Identifier: B278KSP20100E0
• UDI-Public: B278KSP20100E0
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K161520
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 04/06/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/04/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: KSP20100E
• Device Catalogue Number: KSP20100E
• Device Lot Number: 1703580
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 04/06/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 04/28/2017
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: P/N 25001040E ELEOS MALE-FEMALE MIDSECTION 40MM; P/N 25001210E ELEOS TIBIAL POLY SPACER 10MM; P/N 25002101E ELEOS TIBIAL HINGE COMPONENT; P/N 25002114E ELEOS RESURFACING FEMUR AXIAL PIN 4; P/N 25002200E ELEOS PROXIMAL TIBIA 87MM RESECTION; P/N 2500L004E ELEOS RESURFACING FEMUR 4; P/N FS-15120-03M ELEOS CANAL FILLING 15MMX120MM
• Patient Outcome(s): Required Intervention; Hospitalization
• Patient Age: 42 YR
• Patient Sex: Male