MAUDE Adverse Event Report: KEYSTONE DENTAL INC PRIMA PLUS; PRIMA PLUS ?4.1 X 15.0 MM IMPLANT

Model Number	15739K
Medical Device Problem Code	Loss of Osseointegration (2408)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	05/13/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
This mdr was previously submitted to the fda by keystone dental.Complaint (b)(4).
Event or Problem Description
Loss of osseointegration.

• Brand Name: PRIMA PLUS
• Common Device Name: PRIMA PLUS ?4.1 X 15.0 MM IMPLANT
• Manufacturer (Section D): KEYSTONE DENTAL INC; 154 middlesex turnpike; burlington MA 01803
• MDR Report Key: 9659335
• Report Number: 3005990499-2020-15100
• Device Sequence Number: 3475225
• Product Code: DZE
• UDI-Device Identifier: D76815739K0
• UDI-Public: +D76815739K0/$$3221130370406
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: health professional
• Initial Reporter Occupation: Dentist
• Type of Report: Initial
• Report Date (Section B): 12/12/2019

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 Model Number: 15739K
• Device Catalogue Number: 15739K
• Device Lot Number: 37040
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/10/2019
• Initial Report FDA Received Date: 02/03/2020
• 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