FDA Adverse Event Malfunction Summary report: N

BRYAN CERVICAL DISC SYSTEM

MDR report key: 7258603 · Received February 9, 2018

Report

Report Number
1030489-2018-00186
Event Type
Malfunction
Date Received
February 9, 2018
Date of Event
January 19, 2018
Report Date
April 25, 2018
Manufacturer
WARSAW ORTHOPEDICS
Product Code
MJO
PMA / PMN Number
SEE H10
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS PART IS NOT APPROVED FOR USE IN THE US, HOWEVER A LIKE DEVICE WITH PART# 6474525, 510K# P060023 AND UPN (B)(4) IS AVAILABLE FOR THE MARKET. 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. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

VISUAL AND MICROSCOPIC EXAMINATION OF THE -03 MILL GEAR AND -05 MILL PINION INTERFACING FEATURES IDENTIFIED SIGNIFICANT MATERIAL DEFORMATION. THE LOCATION AND NATURE OF THE WEAR IS CONSISTENT WITH INSTRUMENT USAGE. THE ABOVE OBSERVATIONS ARE CONSISTENT WITH ANTICIPATED WEAR. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT WAS PRE-OPERATIVELY DIAGNOSED WITH MYELOPATHY AND DISC DEGENERATION AND UNDERWENT IMPLANTATION OF BRYAN CERVICAL DISC. DURING SURGERY, THE CUTTER DID NOT WORK. IT STARTED TO TURN AT THE BEGINNING BUT THEN IT STOPPED. THE CUTTER WAS THEN REPLACED WITH A NEW ONE. THE PRODUCT CAME IN CONTACT WITH THE PATIENT. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
102383 BRYAN CERVICAL DISC SYSTEM PROSTHESIS, INTERVERTEBRAL DISC MJO WARSAW ORTHOPEDICS NA EM15M055

Patients

Seq Age Sex Outcome Treatment
1