FDA 510(k) Applications Submitted by RITA GIEBEL
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000633 | 02/25/2000 | SYNTHETIC GLASS BONE GRAFT MATERIAL | BLUE SKY BIO |
| K013903 | 11/26/2001 | HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED, VERSION 2 | TRIAD MEDICAL, INC. |
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