ATL Anchors
K-Number: K200503 · 2020-09-02
ApplicantInternational Life Sciences
Decision Date2020-09-02
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
ATL Anchors is a medical device manufactured by International Life Sciences. It received FDA 510(k) clearance on 2020-09-02 under approval number K200503. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ATL Anchors?
ATL Anchors is a medical device that received FDA 510(k) clearance on 2020-09-02. It is manufactured by International Life Sciences. The 510(k) number is K200503.
When was ATL Anchors approved by the FDA?
ATL Anchors received FDA 510(k) clearance on 2020-09-02, under approval number K200503.
What company makes ATL Anchors?
ATL Anchors is manufactured by International Life Sciences.
What is the FDA product code for ATL Anchors?
The FDA product code for ATL Anchors is MBI.
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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.