Lantern® Hip
K-Number: K242616 · 2024-10-03
ApplicantOrthalign, Inc.
Decision Date2024-10-03
Product CodeONN
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Lantern® Hip is a medical device manufactured by Orthalign, Inc.. It received FDA 510(k) clearance on 2024-10-03 under approval number K242616. The device is classified under product code ONN. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Lantern® Hip?
Lantern® Hip is a medical device that received FDA 510(k) clearance on 2024-10-03. It is manufactured by Orthalign, Inc.. The 510(k) number is K242616.
When was Lantern® Hip approved by the FDA?
Lantern® Hip received FDA 510(k) clearance on 2024-10-03, under approval number K242616.
What company makes Lantern® Hip?
Lantern® Hip is manufactured by Orthalign, Inc..
What is the FDA product code for Lantern® Hip?
The FDA product code for Lantern® Hip is ONN.
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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.