VLIFT-s Vertebral Body Replacement System— 510(k) K183071
Substantially EquivalentStryker Spine
FDA 510(k) clearance K183071 for VLIFT-s Vertebral Body Replacement System, Substantially Equivalent on 2019-01-10. Applicant: Stryker Spine. Device class: 2.
Clearance details
- Applicant
- Stryker Spine
- Product code
- Code PLR
- Device class
- Class 2
- Regulation
- 21 CFR 888.3060
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Allendale, NJ, US
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