FDA 510(k)

jFit Surgical Planner

K-Number: K173329 · 2017-11-15

Decision Date2017-11-15

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

jFit Surgical Planner is the device name listed in this FDA 510(k) record. The listed applicant is Jointvue, LLC. It received FDA 510(k) clearance on 2017-11-15 under 510(k) 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. The listed applicant is Jointvue, LLC. The 510(k) number is K173329.

When did jFit Surgical Planner receive FDA 510(k) clearance?

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

Who is the listed applicant for jFit Surgical Planner?

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

What is the FDA product code for jFit Surgical Planner?

The FDA product code for jFit Surgical Planner is LLZ.

Other records listing Jointvue, LLC as applicant

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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.