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FDA 510(k)

Level One Hand Plating System

K-Number: K170124 · 2017-03-09

ApplicantKLS Martin L.P.
Decision Date2017-03-09
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Level One Hand Plating System is a medical device manufactured by KLS Martin L.P.. It received FDA 510(k) clearance on 2017-03-09 under approval number K170124. 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 Level One Hand Plating System?

Level One Hand Plating System is a medical device that received FDA 510(k) clearance on 2017-03-09. It is manufactured by KLS Martin L.P.. The 510(k) number is K170124.

When was Level One Hand Plating System approved by the FDA?

Level One Hand Plating System received FDA 510(k) clearance on 2017-03-09, under approval number K170124.

What company makes Level One Hand Plating System?

Level One Hand Plating System is manufactured by KLS Martin L.P..

What is the FDA product code for Level One Hand Plating System?

The FDA product code for Level One Hand Plating System is HRS.

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Related PubMed Literature

PMID: 42201559 Time-series and thematic analyses of clinical utilities and operational issues in early clinical studies of the da Vinci surgical system. Journal of robotic surgery (2026)

Other Devices by KLS Martin L.P.

K161259KLS Martin Cannulated Headless Screws K161470Internal Distraction - Sterile K151983KLS Martin LSS Plating System K163579KLS Martin Individual Patient Solutions K163315Internal Distraction - Sterile K173320KLS Martin L1 MMF System

View all 11 devices →

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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