Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KLS Martin LSS Plating System

K-Number: K151983 · 2016-04-06

Decision Date2016-04-06
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KLS Martin LSS 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 K151983. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLS Martin LSS Plating System?

KLS Martin LSS 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 K151983.

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

KLS Martin LSS Plating System received FDA 510(k) clearance on 2016-04-06, under approval number K151983.

What company makes KLS Martin LSS Plating System?

KLS Martin LSS Plating System is manufactured by KLS Martin L.P..

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

The FDA product code for KLS Martin LSS Plating System is JDQ.

Other Devices by KLS Martin L.P.

View all 11 devices →

Related Devices (Code: JDQ)

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.