MAUDE Adverse Event Report: NEODENT - JJGC S.A. CM DRIVE ACQUA IMPLANT, TITANIUM, 5.0X18; ENDOSSEOUS DENTAL IMPLANT

Catalog Number	140.898
Medical Device Problem Codes	Failure to Osseointegrate (1863); Loss of Osseointegration (2408)
Health Effect - Clinical Code	Tissue Damage (2104)
Date of Event	01/08/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Exemption number: e2015015.Instradent usa, inc is submitting the report on behalf of neodent - jjgc.
Event or Problem Description
The clinician reports more than 6 months after the dental implant was placed in ada site 4 in type iii bone, the implant had lost osseointegration.The site was not grafted.The product will be forwarded to the manufacturer for investigation.There were no reported complications.
Additional Manufacturer Narrative
Exemption number: e2015015.Instradent usa, inc is submitting the report on behalf of neodent - jjgc after the evaluation, the event was considered as osseointegration failure.The dentist reported that immediate load procedure was performed.
Event or Problem Description
The clinician reports more than 6 months after the dental implant was placed in ada site 4 in type iii bone, the implant had lost osseointegration.The site was not grafted.The product will be forwarded to the manufacturer for investigation.There were no reported complications.(b)(4).

• Brand Name: CM DRIVE ACQUA IMPLANT, TITANIUM, 5.0X18
• Common Device Name: ENDOSSEOUS DENTAL IMPLANT
• Manufacturer (Section D): NEODENT - JJGC S.A.; av. juscelino kubitschek de; oliveira, 3291 cic; curitiba PR 81270 -200; BR 81270-200
• MDR Report Key: 7293543
• Report Number: 3008261720-2018-00830
• Device Sequence Number: 1211669
• Product Code: DZE
• UDI-Device Identifier: 07899878018087
• UDI-Public: 07899878018087
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K150182
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: distributor,foreign
• Initial Reporter Occupation: Dentist
• Type of Report: Initial,Followup
• Report Date (Section B): 02/23/2018
• Report Date (Section F): 01/29/2018

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: Dentist
• Device Expiration Date: 02/04/2019
• Device Catalogue Number: 140.898
• Device Lot Number: 800233686I
• Other Device ID Number: 07899878018087
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/12/2018
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 05/02/2018
• Device Age: 1 MO
• Event Location: Other
• Date Report to Manufacturer: 01/29/2018
• Initial Date Received by Manufacturer: 01/29/2018
• Supplement Date Received by Manufacturer: 04/12/2018
• Initial Report FDA Received Date: 02/23/2018
• Supplement Report FDA Received Date: 05/02/2018
• 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: 74 YR