Venus Basic Spinal Fixation System
by L&K Biomed Co., Ltd. 2 variants
510(k) K103085
Venus Basic Spinal Fixation System is a Class II device made by L&K Biomed Co., Ltd., cleared under FDA 510(k) K103085 on 9 Feb 2011, 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 | NumberK103085 | Date9 Feb 2011 | StatusActive |
Official records
- FDA 510(k) database K103085
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- MNH
- Device class
- Class II
- Regulation
- 21 CFR Part 888.3070
- Advisory committee
- Orthopedic
- FDA decision
- SESE Substantially Equivalent
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