JULIET® LL Lateral Lumbar Cage
K-Number: K161888 · 2016-09-12
ApplicantSpineart
Decision Date2016-09-12
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
JULIET® LL Lateral Lumbar Cage is a medical device manufactured by Spineart. It received FDA 510(k) clearance on 2016-09-12 under approval number K161888. 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 JULIET® LL Lateral Lumbar Cage?
JULIET® LL Lateral Lumbar Cage is a medical device that received FDA 510(k) clearance on 2016-09-12. It is manufactured by Spineart. The 510(k) number is K161888.
When was JULIET® LL Lateral Lumbar Cage approved by the FDA?
JULIET® LL Lateral Lumbar Cage received FDA 510(k) clearance on 2016-09-12, under approval number K161888.
What company makes JULIET® LL Lateral Lumbar Cage?
JULIET® LL Lateral Lumbar Cage is manufactured by Spineart.
What is the FDA product code for JULIET® LL Lateral Lumbar Cage?
The FDA product code for JULIET® LL Lateral Lumbar Cage 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.