MAUDE Adverse Event Report: IMPLANT DIRECT SYBRON MANUFACTURING LLC SIMPLY REACTIVE IMPLANT; DENTAL IMPLANT

Model Number	754708U
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Codes	Failure of Implant (1924); No Consequences Or Impact To Patient (2199)
Date of Event	08/13/2019
Type of Reportable Event	Serious Injury
Event or Problem Description
Per complaint (b)(4), implant failed to integrate.No patient impact was reported.
Additional Manufacturer Narrative
Follow-up submitted to report device evaluation.
Additional Manufacturer Narrative
Follow-up submitted to report correction.Updated section b4 for report submission date and d4 for device information.Updated g1-g2 for follow-up report submitter, g7 for report type and follow-up number.Corrected d4, lot number is corrected to "unknown".

• Brand Name: SIMPLY REACTIVE IMPLANT
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): IMPLANT DIRECT SYBRON MANUFACTURING LLC; 3050 east hillcrest drive; thousand oaks CA 91262
• MDR Report Key: 8977956
• Report Number: 3001617766-2019-02133
• Device Sequence Number: 14276480
• Product Code: DZE
• UDI-Device Identifier: 10841307108139
• UDI-Public: 10841307108139
• Combination Product (Y/N): N
• Initial Reporter State: KY
• Initial Reporter Country: US
• PMA/510(K) Number: K080713
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Dentist
• Remedial Action: Inspection
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 02/12/2020

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?: No
• Operator of Device: Health Professional
• Device Expiration Date: 02/05/2024
• Device Model Number: 754708U
• Device Catalogue Number: 754708U
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/03/2019
• Initial Date Received by Manufacturer: 08/13/2019
• Supplement Date Received by Manufacturer: 09/24/2019; 09/24/2019
• Initial Report FDA Received Date: 09/09/2019
• Supplement Report FDA Received Date: 09/24/2019; 02/12/2020
• 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: 68 YR