DePuy CONDUIT LLIF SQUID Inserter
K-Number: K220449 · 2022-06-28
ApplicantEnztec Limited
Decision Date2022-06-28
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
DePuy CONDUIT LLIF SQUID Inserter is a medical device manufactured by Enztec Limited. It received FDA 510(k) clearance on 2022-06-28 under approval number K220449. 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 DePuy CONDUIT LLIF SQUID Inserter?
DePuy CONDUIT LLIF SQUID Inserter is a medical device that received FDA 510(k) clearance on 2022-06-28. It is manufactured by Enztec Limited. The 510(k) number is K220449.
When was DePuy CONDUIT LLIF SQUID Inserter approved by the FDA?
DePuy CONDUIT LLIF SQUID Inserter received FDA 510(k) clearance on 2022-06-28, under approval number K220449.
What company makes DePuy CONDUIT LLIF SQUID Inserter?
DePuy CONDUIT LLIF SQUID Inserter is manufactured by Enztec Limited.
What is the FDA product code for DePuy CONDUIT LLIF SQUID Inserter?
The FDA product code for DePuy CONDUIT LLIF SQUID Inserter 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.