MAUDE Adverse Event Report: BIOMET 3I FULL OSSEOTITE® IMPLANT 4 X 11.5MM; DENTAL IMPLANT

Model Number	FOS411
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	No Information (3190)
Date of Event	10/29/2009
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Zimmerbiomet complaint number (b)(4).A summary investigation has been completed for lack of primary stability events that do not allege a deficiency with the implant and identified that the reported event is likely due to biological factors which have an adverse effect on implant stability or is related to surgical technique and insertion torque.Due to a wide range of external (non-design/non-manufacturing related), identifying a definitive root cause is generally not possible.Should additional information be received which indicates that the device may have caused or contributed to the event, an additional report will be submitted.Patient identifier unknown / not provided.Age and date of birth unknown / not provided.Weight unknown / not provided.
Event or Problem Description
Customer reported implant was not placed during the surgery due to lack of primary stability.

• Brand Name: FULL OSSEOTITE® IMPLANT 4 X 11.5MM
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): BIOMET 3I; 4555 riverside drive; palm beach gardens FL 33410
• MDR Report Key: 9314248
• Report Number: 0001038806-2019-01346
• Device Sequence Number: 2510137
• Product Code: DZE
• UDI-Device Identifier: 00844868003618
• UDI-Public: (01)00844868003618(10)20090507
• Combination Product (Y/N): N
• PMA/510(K) Number: K063286
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2009
• Device Explanted Year: 2009
• Reporter Type: Manufacturer
• Report Source: foreign,health professional
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 11/12/2019

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: 05/01/2014
• Device Model Number: FOS411
• Device Catalogue Number: FOS411
• Device Lot Number: 2009050712
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 10/15/2019
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/15/2019
• Initial Report FDA Received Date: 11/13/2019
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention