Juliet Ti LL
K-Number: K173702 · 2018-01-03
ApplicantSpineart
Decision Date2018-01-03
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Juliet Ti LL is a medical device manufactured by Spineart. It received FDA 510(k) clearance on 2018-01-03 under approval number K173702. 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 Ti LL?
Juliet Ti LL is a medical device that received FDA 510(k) clearance on 2018-01-03. It is manufactured by Spineart. The 510(k) number is K173702.
When was Juliet Ti LL approved by the FDA?
Juliet Ti LL received FDA 510(k) clearance on 2018-01-03, under approval number K173702.
What company makes Juliet Ti LL?
Juliet Ti LL is manufactured by Spineart.
What is the FDA product code for Juliet Ti LL?
The FDA product code for Juliet Ti LL 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.