FDA 510(k) Applications Submitted by PAMELA SEGALE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K073516 | 12/14/2007 | DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR | KYPHON, INC. |
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