FDA 510(k) Applications Submitted by Alan Burkholder
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K131547 | 05/29/2013 | LANX FUSION SYSTEM | LANX, INC. |
| K082774 | 09/22/2008 | LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE | LANX, LLC |
| K102738 | 09/22/2010 | LANX FUSION SYSTEM | LANX, LLC |
| K123767 | 12/07/2012 | LANX FUSION SYSTEM- SA | LANX, INC. |
| K083815 | 12/22/2008 | LANX FUSION SYSTEM | LANX, INC. |
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