MAUDE manufacturer profile

SYNTHES HAGENDORF · MAX

MAUDE profile for Intervertebral Fusion Device With Bone Graft, Lumbar

Key facts

Manufacturer SYNTHES HAGENDORF
Manufacturer group SYNTHES HAGENDORF
Product code MAX
Product code name Intervertebral Fusion Device With Bone Graft, Lumbar

At a glance

  • 100–999 MAUDE reports
  • 1–9 Death reports
  • 10–99 Injury reports
  • 100–999 Malfunction reports
  • 10–99 Problems flagged by Orca1 signal analytics
  • No Known Impact Or Consequence To Patient, Break, No Patient Involvement, Fitting Problem, Mechanical Jam, Device Operates Differently Than Expected, No Code Available, Separation Failure Most reported problems

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About MAUDE manufacturer and product code profiles

Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.

Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1

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