Vertebral Technologies, Inc.
7 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE (K131540) | Vertebral Technologies, Inc. | 2013-09-03 |
| INTERFUSE T INVERTEBRAL BODY FUSION DEVICE (K110226) | Vertebral Technologies, Inc. | 2011-05-27 |
| INTERFUSE DA INVERTEBRAL BODY FUSION DEVICE (K110045) | Vertebral Technologies, Inc. | 2011-02-03 |
| INTERFUSE T INVERTEBRAL BODY FUSION DEVICE (K102277) | Vertebral Technologies, Inc. | 2010-10-06 |
| INTERFUSE INVERTEBRAL BODY FUSION DEVICE MODEL 9076 (K093675) | Vertebral Technologies, Inc. | 2009-12-23 |
| MODIFICATION TO: INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE , MODEL 9076 (K091988) | Vertebral Technologies, Inc. | 2009-07-30 |
| INTERFUSE INTERVERTEBRAL BODY FUSION DEVICE (K080673) | Vertebral Technologies, Inc. | 2008-06-10 |
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