MAUDE Adverse Event Report: EXACTECH, INC. OPTETRAK LOGIC; LGC TIBIAL FIT TRAY CEM SZ 3F / 3T

Model Number	02-010-03-0330
Medical Device Problem Codes	Adverse Event Without Identified Device or Use Problem (2993); Loosening of Implant Not Related to Bone-Ingrowth (4002)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	06/14/2015
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
This submission represents 1 of 163 events identified via active surveillance activities utilizing data form the (b)(6).Follow-ups for additional information cannot be performed for this complaint as the information was submitted as complete by the registry; there is no identification of facilities or surgeons.All available information about the event and/or patient has been provided and it is not possible to obtain any of the devices.Additional information, including the product investigation, will be submitted within 30 days of receipt.
Event or Problem Description
As reported by (b)(6), this (b)(6), male patient underwent primary total prosthetic replacement using cement of the right knee via medial parapatellar approach on (b)(6) 2013.The indication for the index procedure was osteoarthritis.The patient was implanted with a logic - cruciate retaining - cemented femoral component - right - size 3 (catalog 02-010-03-0330, serial (b)(4)), logic - fit - cemented tibial tray - size 3f/3t (catalog 02-012-45-3030, serial (b)(4)), logic - cruciate retaining tibial insert - size 3 9mm slope + (catalog 02-012-48-3009, serial (b)(4)) and stryker antibiotic loaded medium viscosity bone cement (catalog 61971001, serial (b)(4)).On (b)(6) 2015, approximately 19 months post implantation, the patient underwent revision due to aseptic loosening tibia; instability.The exactech were removed and replaced with no 4 total stabilizer femoral component right, no 4 total stabilizer universal baseplate and no 4 triathlon ts plus tibial insert x3 13mm.
Additional Manufacturer Narrative
The evaluation noted that revision reported was likely the result of an insufficient bond between the implant and the bone, which led to aseptic (non-infected) loosening, possibly secondary to instability.However, the contributions of instability and loosening to the sequence of events cannot be confirmed since the devices were not returned for evaluation and no first hand details were provided.This submission represents 1 of 163 events identified via active surveillance activities utilizing data form the united kingdom national joint registry (uknjr).Follow-ups for additional information cannot be performed for this complaint as the information was submitted as complete by the registry; there is no identification of facilities or surgeons.All available information about the event and/or patient has been provided and it is not possible to obtain any of the devices no information provided.

• Brand Name: OPTETRAK LOGIC
• Common Device Name: LGC TIBIAL FIT TRAY CEM SZ 3F / 3T
• Manufacturer (Section D): EXACTECH, INC.; 2320 nw 66 court; gainesville FL 32653
• MDR Report Key: 9715035
• Report Number: 1038671-2020-00207
• Device Sequence Number: 19367944
• Product Code: JWH
• UDI-Device Identifier: 10885862158116
• UDI-Public: 10885862158116
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K101981
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Device Explanted Year: 2015
• Reporter Type: Manufacturer
• Report Source: company representative,consum
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 05/08/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 10/24/2022
• Device Model Number: 02-010-03-0330
• Device Catalogue Number: 02-012-45-3030
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 01/15/2020
• Supplement Date Received by Manufacturer: 05/04/2020
• Initial Report FDA Received Date: 02/14/2020
• Supplement Report FDA Received Date: 05/08/2020
• 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: Hospitalization; Required Intervention
• Patient Age: 63 YR