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FDA 510(k)

jFit Surgical Planner

K-Number: K173329 · 2017-11-15

ApplicantJointvue, LLC
Decision Date2017-11-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

jFit Surgical Planner is a medical device manufactured by Jointvue, LLC. It received FDA 510(k) clearance on 2017-11-15 under approval number K173329. 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 jFit Surgical Planner?

jFit Surgical Planner is a medical device that received FDA 510(k) clearance on 2017-11-15. It is manufactured by Jointvue, LLC. The 510(k) number is K173329.

When was jFit Surgical Planner approved by the FDA?

jFit Surgical Planner received FDA 510(k) clearance on 2017-11-15, under approval number K173329.

What company makes jFit Surgical Planner?

jFit Surgical Planner is manufactured by Jointvue, LLC.

What is the FDA product code for jFit Surgical Planner?

The FDA product code for jFit Surgical Planner is 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.

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