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FDA 510(k)

VLIFT-s Vertebral Body Replacement System

K-Number: K183071 · 2019-01-10

ApplicantStryker Spine
Decision Date2019-01-10
Product CodePLR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VLIFT-s Vertebral Body Replacement System is a medical device manufactured by Stryker Spine. It received FDA 510(k) clearance on 2019-01-10 under approval number K183071. The device is classified under product code PLR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VLIFT-s Vertebral Body Replacement System?

VLIFT-s Vertebral Body Replacement System is a medical device that received FDA 510(k) clearance on 2019-01-10. It is manufactured by Stryker Spine. The 510(k) number is K183071.

When was VLIFT-s Vertebral Body Replacement System approved by the FDA?

VLIFT-s Vertebral Body Replacement System received FDA 510(k) clearance on 2019-01-10, under approval number K183071.

What company makes VLIFT-s Vertebral Body Replacement System?

VLIFT-s Vertebral Body Replacement System is manufactured by Stryker Spine.

What is the FDA product code for VLIFT-s Vertebral Body Replacement System?

The FDA product code for VLIFT-s Vertebral Body Replacement System is PLR.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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