InjuryGXN
ACCUSHAPE PEEK
Received Jul 17, 2026
Report 3009196021-2026-00011 · MDR key 25864426
Device
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
Not reported
- Unspecified Infection
Narrative
Description of Event or Problem
CRANIAL DEVICE EXPLANT.
Additional Manufacturer Narrative
ADDITIONAL INFORMATION LIKE PATIENT'S WEIGHT AND INFECTION CAUSE/TYPE WAS REQUESTED, BUT THE SALES REPRESENTATIVE WAS NOT ABLE TO PROVIDE THE REQUESTED INFORMATION.