VMA System version 3.0
K-Number: K172327 · 2017-08-25
ApplicantOrtho Kinematics, Inc.
Decision Date2017-08-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
VMA System version 3.0 is a medical device manufactured by Ortho Kinematics, Inc.. It received FDA 510(k) clearance on 2017-08-25 under approval number K172327. 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 VMA System version 3.0?
VMA System version 3.0 is a medical device that received FDA 510(k) clearance on 2017-08-25. It is manufactured by Ortho Kinematics, Inc.. The 510(k) number is K172327.
When was VMA System version 3.0 approved by the FDA?
VMA System version 3.0 received FDA 510(k) clearance on 2017-08-25, under approval number K172327.
What company makes VMA System version 3.0?
VMA System version 3.0 is manufactured by Ortho Kinematics, Inc..
What is the FDA product code for VMA System version 3.0?
The FDA product code for VMA System version 3.0 is LLZ.
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Official Source
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