MAUDE Adverse Event Report: WARSAW ORTHOPEDICS CD HORIZON; APPLIANCE, FIXATION, SPINAL INTERLAMINAL

Catalog Number	86946540
Medical Device Problem Code	Failure to Align (2522)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	08/17/2016
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Neither the device nor films of applicable imaging studies were returned to the manufacturer for evaluation.Therefore, we are unable to determine the definitive cause of the reported event.
Event or Problem Description
It was reported that the patient underwent an unspecified procedure due to lumbar inter-vertebral disc degeneration.During procedure, the device was found slipped and could not be used anymore.The surgeon had to replace it with new one to complete the surgery.The device came in contact with the patient.No patient complications were reported as a result of the event.
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.

• Brand Name: CD HORIZON
• Common Device Name: APPLIANCE, FIXATION, SPINAL INTERLAMINAL
• Manufacturer (Section D): WARSAW ORTHOPEDICS; 2500 silveus crossing; warsaw IN 46582
• MDR Report Key: 6101333
• Report Number: 1030489-2016-03129
• Device Sequence Number: 19076249
• Product Code: KWP
• UDI-Device Identifier: 00885074171067
• UDI-Public: 00885074171067
• Combination Product (Y/N): N
• Initial Reporter Country: CH
• PMA/510(K) Number: K981676
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 10/17/2016

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 Catalogue Number: 86946540
• Device Lot Number: 0347654W
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 10/17/2016
• Supplement Date Received by Manufacturer: 10/17/2016
• Initial Report FDA Received Date: 11/15/2016
• Supplement Report FDA Received Date: 09/26/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 60 YR