FDA 510(k) Applications Submitted by DREW JOHNSON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990469 | 02/16/1999 | LAMITRODE LEADS | ADVANCED NEUROMODULATION SYSTEMS |
| K030674 | 03/04/2003 | MODIFICATION TO AXXESS SPINAL CORD STIMULATION LEAD | ADVANCED NEUROMODULATION SYSTEMS |
| K953838 | 08/16/1995 | MYOCARDIAL PROTECTION SYSTEM | QUEST MEDICAL, INC. |
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