FDA 510(k)

JointPoint

K-Number: K160284 · 2016-08-03

Decision Date2016-08-03

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

JointPoint is the device name listed in this FDA 510(k) record. The listed applicant is Jointpoint, Inc.. It received FDA 510(k) clearance on 2016-08-03 under 510(k) 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. The listed applicant is Jointpoint, Inc.. The 510(k) number is K160284.

When did JointPoint receive FDA 510(k) clearance?

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

Who is the listed applicant for JointPoint?

The FDA 510(k) record lists Jointpoint, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JointPoint?

The FDA product code for JointPoint is LLZ.

Related Devices (Code: LLZ)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.