MAUDE Adverse Event Report: JJGC S.A. CM DRIVE IMPLANT, TITANIUM, 5.0X8 MM; ENDOSSEOUS DENTAL IMPLANT

Model Number	109.1002
Medical Device Problem Code	Failure to Osseointegrate (1863)
Health Effect - Clinical Codes	Sinus Perforation (2277); Fibrosis (3167)
Date of Event	07/05/2021
Type of Reportable Event	Serious Injury
Event or Problem Description
The clinician reports the implant was inserted (b)(6) 2021 in ada 3.Details of surgery: primary stability not achieved, implant surface not completely covered with bone and sinus perforation.On (b)(6) 2021, non-osseointegration was verified.Patient presented with bone type iv, fair oral hygiene, bruxism and inadequate bone quality/quantity.The device was forwarded to the manufacturer.At the event the patient experienced: mobility.No further patient complications were reported.

• Brand Name: CM DRIVE IMPLANT, TITANIUM, 5.0X8 MM
• Common Device Name: ENDOSSEOUS DENTAL IMPLANT
• Manufacturer (Section D): JJGC S.A.; av. juscelino kubitschek de; oliveira, 3291 cic; curitiba PR 81270 -200; BR 81270-200
• MDR Report Key: 12563308
• Report Number: 0001222315-2021-16312
• Device Sequence Number: 13787281
• Product Code: DZE
• UDI-Device Identifier: 07899878023418
• UDI-Public: 07899878023418
• Combination Product (Y/N): N
• Initial Reporter State: OR
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): N
• Reporter Type: Importer
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 10/01/2021
• Report Date (Section F): 09/07/2021

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: 10/26/2022
• Device Model Number: 109.1002
• Device Catalogue Number: 109.1002
• Device Lot Number: 115778I
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/07/2021
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 10/01/2021
• Device Age: 45 MO
• Event Location: Other
• Date Report to Manufacturer: 09/07/2021
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 10/01/2021
• 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: 57 YR