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FDA 510(k)

JointPoint

K-Number: K160284 · 2016-08-03

ApplicantJointpoint, Inc.
Decision Date2016-08-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JointPoint is a medical device manufactured by Jointpoint, Inc.. It received FDA 510(k) clearance on 2016-08-03 under approval number K160284. 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 JointPoint?

JointPoint is a medical device that received FDA 510(k) clearance on 2016-08-03. It is manufactured by Jointpoint, Inc.. The 510(k) number is K160284.

When was JointPoint approved by the FDA?

JointPoint received FDA 510(k) clearance on 2016-08-03, under approval number K160284.

What company makes JointPoint?

JointPoint is manufactured by Jointpoint, Inc..

What is the FDA product code for JointPoint?

The FDA product code for JointPoint is LLZ.

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Official Source

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