MAUDE Adverse Event Report: GLOBUS MEDICAL, INC. ELSA; ELSA SPACER 20 X 50MM, 8-17MM, 5-20°

Model Number	1122.1050
Health Effect - Clinical Code	Insufficient Information (4580)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device was not available for evaluation as it remains in the patient.Imaging provided does not clearly show a loss of implant height.The images are aligned differently skewing the orientation and perception of the height.The exact cause of the reported issue could not be determined.
Event or Problem Description
It was reported that an elsa spacer has collapsed post-operatively.There are no plans for a revision surgery.

• Brand Name: ELSA
• Common Device Name: ELSA SPACER 20 X 50MM, 8-17MM, 5-20°
• Manufacturer (Section D): GLOBUS MEDICAL, INC.; 2560 general armistead avenue; audubon 19403
• MDR Report Key: 11440245
• Report Number: 3004142400-2021-00041
• Device Sequence Number: 3997732
• Product Code: OVD
• UDI-Device Identifier: 00889095334425
• UDI-Public: 00889095334425
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K161379
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 03/05/2021

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 Model Number: 1122.1050
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/08/2021
• Initial Report FDA Received Date: 03/08/2021
• 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: Other