FDA 510(k) Applications Submitted by Glenn Stiegman
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K101310 | 05/11/2010 | VU APOD INTERVERTEBRAL BODY FUSION DEVICE | THEKEN SPINE LLC |
| K101363 | 05/14/2010 | VU CPOD INTERVERTEBRAL BODU FUSION DEVICE | MUSCULOSKELETAL CLINICAL REGULATORY ADVISERS |
| K071990 | 07/20/2007 | VALEO CERVICAL PLATE SYSTEM | AMEDICA CORP. |
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