Lucent® XP
K-Number: K182584 · 2018-12-10
ApplicantSpinal Elements, Inc.
Decision Date2018-12-10
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Lucent® XP is a medical device manufactured by Spinal Elements, Inc.. It received FDA 510(k) clearance on 2018-12-10 under approval number K182584. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Lucent® XP?
Lucent® XP is a medical device that received FDA 510(k) clearance on 2018-12-10. It is manufactured by Spinal Elements, Inc.. The 510(k) number is K182584.
When was Lucent® XP approved by the FDA?
Lucent® XP received FDA 510(k) clearance on 2018-12-10, under approval number K182584.
What company makes Lucent® XP?
Lucent® XP is manufactured by Spinal Elements, Inc..
What is the FDA product code for Lucent® XP?
The FDA product code for Lucent® XP is MAX.
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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.