WEBER PERMALOCK — Allo Pro Corp. (510(k) K896669)
WEBER PERMALOCK — Allo Pro Corp. (510(k) K896669) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: WEBER PERMALOCK; Applicant: Allo Pro Corp.; Clearance track: 510(k).
| Device name | WEBER PERMALOCK |
|---|---|
| Applicant | Allo Pro Corp. |
| Clearance track | 510(k) |
| Submission number | K896669 |
| Decision | Substantially Equivalent for Some Indications |
| Decision date | 1990-02-06 |
| Date received | 1989-11-27 |
| Product code | LZO |
| Device class | 2 |
| Medical specialty | Orthopedic |
| Applicant location | FL, US |
| Source | openFDA device |
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$1999/mo
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