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Home » FDA: Test 'Worst-Case' Version of Intervertebral Body Fusion Devices
FDA: Test 'Worst-Case' Version of Intervertebral Body Fusion Devices
August 2, 2007
Manufacturers of intervertebral body fusion devices containing bone-grafting material should test constructs representing the worst-case (e.g., most likely to fail) final design version, the FDA says in a recent guidance document.