Skip to content

InterFuse S 9076-09-20-5Recalls & reported problems

Next Orthosurgical, Inc. · Intervertebral Body Fusion Device · Class 2 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00819475010090), received between Nov 9, 2015 and Nov 9, 2015 — classified as 1 injury.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Migration or Expulsion of Device1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 9, 2015Migration or Expulsion of Device

    DURING A REGULAR 6 WEEK POST-OP FOLLOW-UP VISIT ON (B)(6), 2015, AN X-RAY REVEALED A MODULE MIGRATION. THE PATIENT WAS ASYMPTOMATIC, WITH NO NEUROLOGIC SYMPTOMS. SURGERY WAS PERFORMED ON (B)(6), 2015 TO REMOVE THE MIGRATED MODULE (A "C" MODULE). THE REMAINING CONSTRUCT WAS INTACT AND NO ADDITIONAL ACTION WAS REQUIRED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5212196 ↗

Other Intervertebral Fusion Device With Bone Graft, Lumbar devices

All Intervertebral Fusion Device With Bone Graft, Lumbar devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.