ProLift Lateral Fixated
K-Number: K200338 · 2020-04-17
ApplicantLife Spine, Inc.
Decision Date2020-04-17
Product CodeOVD
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
ProLift Lateral Fixated is a medical device manufactured by Life Spine, Inc.. It received FDA 510(k) clearance on 2020-04-17 under approval number K200338. The device is classified under product code OVD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ProLift Lateral Fixated?
ProLift Lateral Fixated is a medical device that received FDA 510(k) clearance on 2020-04-17. It is manufactured by Life Spine, Inc.. The 510(k) number is K200338.
When was ProLift Lateral Fixated approved by the FDA?
ProLift Lateral Fixated received FDA 510(k) clearance on 2020-04-17, under approval number K200338.
What company makes ProLift Lateral Fixated?
ProLift Lateral Fixated is manufactured by Life Spine, Inc..
What is the FDA product code for ProLift Lateral Fixated?
The FDA product code for ProLift Lateral Fixated is OVD.
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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.