MAUDE Adverse Event Report: MDT SOFAMOR DANEK PUERTO RICO CD HORIZON SOLERA VOYAGER SPINAL SYSTEM; ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

Catalog Number	54750017540
Medical Device Problem Code	Loosening of Implant Not Related to Bone-Ingrowth (4002)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product analysis: a microscopic review of the bone screw show heavy witness marks on one side and little to no witness marks on the other side.There is an indication that the rod was angulated in the bone screw head.There are faint witness marks of the rod on installation but no signs of failure.The rods being angulated in the head of the bone screw could lead to the screw backing out over time.If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
Procedure: minimally invasive spinal transforaminal lumbar interbody fusion (tlif) pre-operative diagnosis: neurological symptom it was reported that post-op, screw was loose.Revision surgery was performed due to screw loosing.The product came in contact with the patient.There were no complications as a result of this event.

• Brand Name: CD HORIZON SOLERA VOYAGER SPINAL SYSTEM
• Common Device Name: ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE
• Manufacturer (Section D): MDT SOFAMOR DANEK PUERTO RICO; barrio marianna rd 909, km0.4; humacao PR 00792
• MDR Report Key: 8347497
• Report Number: 1030489-2019-00165
• Device Sequence Number: 1915274
• Product Code: NKB
• UDI-Device Identifier: 00643169501133
• UDI-Public: 00643169501133
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K143375
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 02/18/2019

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?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 04/20/2025
• Device Catalogue Number: 54750017540
• Device Lot Number: H5356296
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/16/2019
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/23/2019
• Initial Report FDA Received Date: 02/18/2019
• 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