FDA 510(k) Applications Submitted by STEVEN BUCKLEY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K983161 | 09/09/1998 | KURER CROWN SAVER K4 ANCHOR SYSTEM-THE UNIVERSAL KIT, KURER STANDARD K4 ANCHOR SYSTEM- THE READY CORE KIT, KURER FIN-LOC | SABRE-K LTD. |
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