FDA 510(k) Applications Submitted by LDR SPINE USA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K161798 | 06/30/2016 | FacetBRIDGE« System | LDR SPINE USA, INC. |
| K162133 | 08/01/2016 | VerteFIT Corpectomy Cage System | LDR SPINE USA, INC. |
| K161173 | 04/26/2016 | Avenue« T TLIF Cage | LDR SPINE USA, INC. |
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