ROCCIA® MultiLIF
510(k) K171434
ROCCIA® MultiLIF is a Class II device made by Silony Medical GmbH, cleared under FDA 510(k) K171434 on 21 Dec 2017, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK171434 | Date21 Dec 2017 | StatusActive |
Official records
- FDA 510(k) database K171434
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MAX
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3080
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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