FDA 510(k) Applications Submitted by MEDITECH ADVISORS, LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090707 | 03/17/2009 | TALOS INTERVERTEBRAL BODY FUSION DEVICE | MEDITECH ADVISORS, LLC |
| K122850 | 09/18/2012 | TALOS-C CERVICAL INTERVERTEBRAL BODY FUSION DEVICES | MEDITECH ADVISORS, LLC |
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