OrthoView 7.2
K-Number: K171068 · 2017-10-18
ApplicantMeridian Technique, Ltd.
Decision Date2017-10-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
OrthoView 7.2 is a medical device manufactured by Meridian Technique, Ltd.. It received FDA 510(k) clearance on 2017-10-18 under approval number K171068. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the OrthoView 7.2?
OrthoView 7.2 is a medical device that received FDA 510(k) clearance on 2017-10-18. It is manufactured by Meridian Technique, Ltd.. The 510(k) number is K171068.
When was OrthoView 7.2 approved by the FDA?
OrthoView 7.2 received FDA 510(k) clearance on 2017-10-18, under approval number K171068.
What company makes OrthoView 7.2?
OrthoView 7.2 is manufactured by Meridian Technique, Ltd..
What is the FDA product code for OrthoView 7.2?
The FDA product code for OrthoView 7.2 is LLZ.
Related Devices (Code: LLZ)
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.