inforMED
InjuryKWQ

ABC

Received Jul 6, 2026

Report 3005673311-2026-00139 · MDR key 25725128

Device

Generic name

Appliance, Fixation, Spinal Intervertebral Body

Manufacturer

Aesculap Ag

Product problems

  • Insufficient Device Problem Information

Patient

NA · Unknown

  • Insufficient Information

Narrative

Description of Event or Problem

IT WAS REPORTED THAT DRIVERS WERE IN NEED FOR THE REMOVAL OF ABC AND ABC 2 PLATES. ADDITIONAL INFORMATION WAS REQUESTED BUT NOT PROVIDED. THIS REPORT IS FILED UNDER AIS REFERENCE (B)(4).