MAUDE Adverse Event Report: BIOMET 3I OSSEOTITE IMPLANT 4 X 13MM; DENTAL IMPLANT

Model Number	OSS413
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Information (3190)
Date of Event	03/03/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Zimmer biomet (b)(4).Patient identifier unknown / not provided.Weight unknown / not provided.Email address unknown / not provided.
Event or Problem Description
It was reported that the neck portion of the implant fractured.Implant was completely removed.
Event or Problem Description
No further event information is available at the time of this report.
Additional Manufacturer Narrative
Zimmerbiomet complaint number (b)(4).The osseotite® implant 4 x 13mm (oss413) was not returned.Since product has not been returned, visual/functional inspection could not be performed.The investigation has been performed based on the available information.No pre-existing conditions were noted on the product experience report(per).The reported product was located on tooth # 36 (fdi) and used for approximately 17 years.The reported event could not be recreated due to the nature of the dental device and event (fracture).The customer has not provided additional pictures or x-ray images of the product.Dhr review was completed for the subject lot number 179181.It was confirmed that all operations and inspections were executed as per applicable procedure.No deviations or non-conformances, which could have caused or contributed to the reported event was noted as part of the dhr.Lot was inspected and passed all acceptance criteria by qa.Complaint history review was performed for the reported lot number (179181) for similar event and no other complaint was identified within the past two years.April post market trending was reviewed and there were no actionable events or corrective actions for the reported event (implant fracture) or product (oss413).Therefore, based on the available information, device malfunction could not be verified and the reported event was non-verifiable.The following sections have been updated: h3: device evaluated by manufacturer: change ¿no' to 'yes.'.
Additional Manufacturer Narrative
Zimmerbiomet complaint number (b)(4).One osseotite® implant 4 x 13mm (oss413) was returned for inspection.Visual evaluation of the returned device notes that the implant is covered in a large volume of bone at the threads, and fractured at the collar into two pieces.No pre-existing conditions were noted on the per.The reported product was located on tooth # 36 (fdi) and used for approximately 17 years.The reported event could not be recreated due to the nature of the dental device and event (fracture).The customer has not provided additional pictures or x-ray images of the product.Dhr review was completed for the subject lot number 179181.It was confirmed that all operations and inspections were executed as per applicable procedure.No deviations or non-conformances, which could have caused or contributed to the reported event was noted as part of the dhr.Lot was inspected and passed all acceptance criteria by qa.Complaint history review was performed for the reported lot number (179181) for similar event and no other complaint was identified within the past two years.May post market trending was reviewed and there were no actionable events or corrective actions for the reported event (implant fracture) or product (oss413).Therefore, based on the available information, device malfunction has occurred and the reported event was confirmed.The following sections have been updated: b4: date of this report.B5: describe event or problem.G4: date received by manufacturer.G7: type of report, follow-up number.H2: follow up type.H3: device evaluated by manufacturer: change ¿no' to 'yes.' h6: evaluation codes.H10: additional narrative.
Event or Problem Description
No further event information is available at the time of this report.

• Brand Name: OSSEOTITE IMPLANT 4 X 13MM
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): BIOMET 3I; 4555 riverside drive; palm beach gardens FL 33410
• MDR Report Key: 9876939
• Report Number: 0001038806-2020-00566
• Device Sequence Number: 18973048
• Product Code: DZE
• UDI-Device Identifier: 00844868013198
• UDI-Public: (01)00844868013198(17)071231(10)179181(241)OSS413
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: K063286
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2003
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: foreign,user facility
• Initial Reporter Occupation: Dentist
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 07/31/2020

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?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 12/31/2007
• Device Model Number: OSS413
• Device Catalogue Number: OSS413
• Device Lot Number: 179181
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/05/2020
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 03/05/2020
• Supplement Date Received by Manufacturer: 06/16/2020; 07/28/2020
• Initial Report FDA Received Date: 03/25/2020
• Supplement Report FDA Received Date: 06/25/2020; 07/31/2020
• 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: Required Intervention
• Patient Age: 70 YR