MAUDE Adverse Event Report: SPINAL KINETICS M6-C; ARTIFICIAL CERVICAL DISC

Device Problem Patient-Device Incompatibility (2682)

Patient Problem Insufficient Information (4580)

Event Type  Injury  

Manufacturer Narrative

The device was not received for evaluation.No device identifiers; serial number, lot number, were provided therefore a review of the lot history records could not be performed.A review of the risk management file resulted in no new risk associated with the device.Rmf 0003 rev 36 line 12.75 - device explanted.

Event Description

Information provided via abstract publication states that m6 implanted at c5/6 in (b)(6) 2014 and another m6 implanted at c6/7 in (b)(6) 2016.The device at c5/6 failed-- both devices were removed in (b)(6) 2023.No leukocytes, aerobic or anaerobic growth.Foreign body reaction at c5/6 and c6/7.Levels.

• Brand Name: M6-C
• Type of Device: ARTIFICIAL CERVICAL DISC
• Manufacturer (Section D): SPINAL KINETICS; 501 mercury drive; sunnyvale CA 94085
• Manufacturer (Section G): SPINAL KINETICS; 501 mercury drive; sunnyvale CA 94085
• Manufacturer Contact: ehab esmail ; 501 mercury drive; sunnyvale, CA 94085 ; 2149372015
• MDR Report Key: 17373955
• MDR Text Key: 319551735
• Report Number: 3004987282-2023-00036
• Device Sequence Number: 1
• Product Code: MJO
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: P170036
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Literature,Health Professional
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 07/17/2023

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
• Device Operator: Lay User/Patient
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 06/27/2023
• Initial Date FDA Received: 07/21/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Age: 46 YR
• Patient Sex: Male