Delta Dual Mobility System
K-Number: K181491 · 2019-05-09
ApplicantLima Corporate S.P.A.
Decision Date2019-05-09
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Delta Dual Mobility System is a medical device manufactured by Lima Corporate S.P.A.. It received FDA 510(k) clearance on 2019-05-09 under approval number K181491. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Delta Dual Mobility System?
Delta Dual Mobility System is a medical device that received FDA 510(k) clearance on 2019-05-09. It is manufactured by Lima Corporate S.P.A.. The 510(k) number is K181491.
When was Delta Dual Mobility System approved by the FDA?
Delta Dual Mobility System received FDA 510(k) clearance on 2019-05-09, under approval number K181491.
What company makes Delta Dual Mobility System?
Delta Dual Mobility System is manufactured by Lima Corporate S.P.A..
What is the FDA product code for Delta Dual Mobility System?
The FDA product code for Delta Dual Mobility System is LZO.
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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.