K IISCHZ FEB[removed]PERIMETER® Interhody Fusion Device 510(k) Summary

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Date: 2012-03-26 00:31:44 Food law Medical equipment Medical device Medical technology Federal Food Drug and Cosmetic Act Premarket approval Spondylolisthesis Center for Devices and Radiological Health Title 21 of the Code of Federal Regulations Medicine Health Food and Drug Administration		K IISCHZ FEB[removed]PERIMETER® Interhody Fusion Device 510(k) Summary Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 197,49 KB Share Document on Facebook

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