LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002 — Laurimed, LLC (510(k) K082194)
LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002 — Laurimed, LLC (510(k) K082194) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002; Applicant: Laurimed, LLC; Clearance track: 510(k).
| Device name | LAURIMED PERCUTANEOUS DISCECTOMY SYSTEM, MODEL FG-000002 |
|---|---|
| Applicant | Laurimed, LLC |
| Clearance track | 510(k) |
| Submission number | K082194 |
| Decision | Substantially Equivalent |
| Decision date | 2008-08-28 |
| Date received | 2008-08-04 |
| Product code | HRX |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | CA, US |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →