BridalVeil Navigated Instruments
K-Number: K182982 · 2019-01-04
ApplicantAstura Medical
Decision Date2019-01-04
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
BridalVeil Navigated Instruments is a medical device manufactured by Astura Medical. It received FDA 510(k) clearance on 2019-01-04 under approval number K182982. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the BridalVeil Navigated Instruments?
BridalVeil Navigated Instruments is a medical device that received FDA 510(k) clearance on 2019-01-04. It is manufactured by Astura Medical. The 510(k) number is K182982.
When was BridalVeil Navigated Instruments approved by the FDA?
BridalVeil Navigated Instruments received FDA 510(k) clearance on 2019-01-04, under approval number K182982.
What company makes BridalVeil Navigated Instruments?
BridalVeil Navigated Instruments is manufactured by Astura Medical.
What is the FDA product code for BridalVeil Navigated Instruments?
The FDA product code for BridalVeil Navigated Instruments is OLO.
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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.