inforMED
InjuryEZX

OPTIMESH 1500-E

Received Jan 28, 2015 · Event occurred Dec 29, 2014

Report 2135156-2015-00001 · MDR key 4469169

Device

Manufacturer

Spineology, Inc.

Model number

1500-E

Catalog number

330-2050

Lot number

S14087

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

NA

  • Pain

Narrative

Description of Event or Problem

SURGEON PERFORMED L4-5/L5-S1 FUSION ON (B)(6) 2014. APPROXIMATELY ONE WEEK POST-OP, PATIENT DEVELOPED LLE PAIN, CONSISTENT WITH L SIDED L4-5 APPROACH. MRI INDICATED BONE/MESH IN THE FORAMEN. ON (B)(6) 2014, SURGERY WAS PERFORMED TO EXCISE BONE/MESH FROM FORAMEN. PATIENT HAS NOT REPORTED ANY NEW OR RESIDUAL SYMPTOMS POSTOPERATIVELY.