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

Catalog Number	403716
Medical Device Problem Code	Separation Problem (4043)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	07/25/2018
Type of Reportable Event	Malfunction
Event or Problem Description
Per complaint (b)(4), during the osteotomy, the implant became stuck midway.The doctor was unable to remove the implant without damaging the implant or instruments.There was no adverse impact to patient.
Event or Problem Description
Per complaint (b)(4), during the osteotomy, the implant became stuck midway.The doctor was unable to remove the implant without damaging the implant or instruments.There was no adverse impact to patient.

• Brand Name: SCREWINDIRECT IMPLANT
• Common Device Name: DENTAL IMPLANT
• Manufacturer (Section D): IMPLANT DIRECT SYBRON MANUFACTURING LLC; 3050 east hillcrest drive; thousand oaks CA 91362
• MDR Report Key: 7853733
• Report Number: 3001617766-2018-00219
• Device Sequence Number: 1981008
• Product Code: DZE
• UDI-Device Identifier: 10841307104797
• UDI-Public: 10841307104797
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K061319
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Dentist
• Remedial Action: Inspection
• Type of Report: Initial,Followup
• Report Date (Section B): 09/07/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 03/27/2022
• Device Catalogue Number: 403716
• Device Lot Number: 92089
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/22/2018
• Initial Date Received by Manufacturer: 08/09/2018
• Supplement Date Received by Manufacturer: 08/09/2018
• Initial Report FDA Received Date: 09/06/2018
• Supplement Report FDA Received Date: 09/07/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 68 YR