DeviceClearance

VLIFT-s Vertebral Body Replacement System— 510(k) K183071

Substantially Equivalent

Stryker Spine

FDA 510(k) clearance K183071 for VLIFT-s Vertebral Body Replacement System, Substantially Equivalent on 2019-01-10. Applicant: Stryker Spine.

Clearance details

Applicant
Stryker Spine
Product code
Code PLR
Advisory panel
Orthopedic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Allendale, NJ, US
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.