FDA 510(k) Applications Submitted by ADVANCED NEUROMODULATION SYSTEM,INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K022222 | 07/09/2002 | LAMITRODE S-SERIES (S4 AND S8) LEADS | ADVANCED NEUROMODULATION SYSTEM,INC |
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