TRIDENT ANCHOR — Johnson & Johnson Company (510(k) K060914)
TRIDENT ANCHOR — Johnson & Johnson Company (510(k) K060914) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: TRIDENT ANCHOR; Applicant: Johnson & Johnson Company; Clearance track: 510(k).
| Device name | TRIDENT ANCHOR |
|---|---|
| Applicant | Johnson & Johnson Company |
| Clearance track | 510(k) |
| Submission number | K060914 |
| Decision | Substantially Equivalent |
| Decision date | 2006-06-09 |
| Date received | 2006-04-04 |
| Product code | HWC |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | MA, US |
| Source | openFDA device |
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$1999/mo
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