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FDA 510(k)

KLS Martin Thoracic Plating System

K-Number: K153482 · 2016-04-06

ApplicantKLS-Martin L.P.
Decision Date2016-04-06
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KLS Martin Thoracic Plating System is a medical device manufactured by KLS-Martin L.P.. It received FDA 510(k) clearance on 2016-04-06 under approval number K153482. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLS Martin Thoracic Plating System?

KLS Martin Thoracic Plating System is a medical device that received FDA 510(k) clearance on 2016-04-06. It is manufactured by KLS-Martin L.P.. The 510(k) number is K153482.

When was KLS Martin Thoracic Plating System approved by the FDA?

KLS Martin Thoracic Plating System received FDA 510(k) clearance on 2016-04-06, under approval number K153482.

What company makes KLS Martin Thoracic Plating System?

KLS Martin Thoracic Plating System is manufactured by KLS-Martin L.P..

What is the FDA product code for KLS Martin Thoracic Plating System?

The FDA product code for KLS Martin Thoracic Plating System is HRS.

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Other Devices by KLS-Martin L.P.

K181241KLS Martin Individual Patient Solutions (IPS) Planning System K180962KLS Martin Individual Patient Solutions 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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Related Devices (Code: HRS)

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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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