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Vertebral Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K131540	INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE	MAX	2013-09-03	View
510(k)	K110226	INTERFUSE T INVERTEBRAL BODY FUSION DEVICE	MAX	2011-05-27	View
510(k)	K110045	INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE	MAX	2011-02-03	View
510(k)	K102277	INTERFUSE T INVERTEBRAL BODY FUSION DEVICE	MAX	2010-10-06	View
510(k)	K093675	INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076	MAX	2009-12-23	View
510(k)	K091988	MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076	MAX	2009-07-30	View
510(k)	K080673	INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE	MAX	2008-06-10	View

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