MAUDE manufacturer profile

ZAVATION MEDICAL PRODUCTS, LLC · MAX

MAUDE profile for Intervertebral Fusion Device With Bone Graft, Lumbar

Key facts

Manufacturer ZAVATION MEDICAL PRODUCTS, LLC
Manufacturer group ZAVATION MEDICAL PRODUCTS, LLC
Product code MAX
Product code name Intervertebral Fusion Device With Bone Graft, Lumbar

At a glance

  • 1–9 MAUDE reports
  • 1–9 Injury reports
  • 1–9 Malfunction reports
  • 1–9 Problems flagged by Orca1 signal analytics
  • Collapse, Migration, Patient Device Interaction Problem, Nicks, cuts or tears of dura or other tissues by device, Unspecified Nervous System Problem, Ambulation Difficulties, Inadequate Osseointegration 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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