REVISION PROTHESIS — Smith & Nephew, Inc. (510(k) K110837)
REVISION PROTHESIS — Smith & Nephew, Inc. (510(k) K110837) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: REVISION PROTHESIS; Applicant: Smith & Nephew, Inc.; Clearance track: 510(k).
| Device name | REVISION PROTHESIS |
|---|---|
| Applicant | Smith & Nephew, Inc. |
| Clearance track | 510(k) |
| Submission number | K110837 |
| Decision | Substantially Equivalent |
| Decision date | 2011-04-22 |
| Date received | 2011-03-25 |
| Product code | JWH |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | TN, US |
| Source | openFDA device |
🔍 Search all device clearances →
$1999/mo
Try DeviceClear →