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FDA 510(k)

KLS Martin Individual Patient Solutions

K-Number: K180962 · 2018-08-13

ApplicantKLS-Martin L.P.
Decision Date2018-08-13
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KLS Martin Individual Patient Solutions is a medical device manufactured by KLS-Martin L.P.. It received FDA 510(k) clearance on 2018-08-13 under approval number K180962. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLS Martin Individual Patient Solutions?

KLS Martin Individual Patient Solutions is a medical device that received FDA 510(k) clearance on 2018-08-13. It is manufactured by KLS-Martin L.P.. The 510(k) number is K180962.

When was KLS Martin Individual Patient Solutions approved by the FDA?

KLS Martin Individual Patient Solutions received FDA 510(k) clearance on 2018-08-13, under approval number K180962.

What company makes KLS Martin Individual Patient Solutions?

KLS Martin Individual Patient Solutions is manufactured by KLS-Martin L.P..

What is the FDA product code for KLS Martin Individual Patient Solutions?

The FDA product code for KLS Martin Individual Patient Solutions is JEY.

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Related PubMed Literature

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Other Devices by KLS-Martin L.P.

K153482KLS Martin Thoracic Plating System K181241KLS Martin Individual Patient Solutions (IPS) Planning System K191028KLS Martin Individual Patient Solutions K182889KLS Martin Individual Patient Solutions (IPS) Planning System K182789KLS Martin Individual Patient Solutions (IPS) Planning System K201052KLS Martin Individual Patient Solutions (IPS) Planning System

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Official Source

View on FDA Database →

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

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