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FDA 510(k)

KLS Martin LSS Plating System

K-Number: K151983 · 2016-04-06

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

Device Summary

KLS Martin LSS Plating System is the device name listed in this FDA 510(k) record. The listed applicant is KLS Martin L.P.. It received FDA 510(k) clearance on 2016-04-06 under 510(k) 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. The listed applicant is KLS Martin L.P.. The 510(k) number is K151983.

When did KLS Martin LSS Plating System receive FDA 510(k) clearance?

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

Who is the listed applicant for KLS Martin LSS Plating System?

The FDA 510(k) record lists KLS Martin L.P. as the applicant. This does not by itself establish the device manufacturer.

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 records listing KLS Martin L.P. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254162KLS Martin Ixos SystemK253660KLS Martin Pure Pectus SystemK250988KLS Martin Pure Pectus SystemK250865KLS Martin IPS Forearm SystemK252573KLS Martin Cranial Implants - MR Conditional; K944565: KLS-Martin Micro Osteosynthesis System (1.5MM); K971297: KLS Martin Centre-Drive Drill-Free Screw; K060177: KLS Martin Rigid Fixation - Sterile; K062570: Individual Patient Solutions - Ti (IPS-Ti); K072707: Individual Patient Solutions - PEEK (IPS-PEEK) ; K151382: Individual Patient Solutions - (IPS-PEEK) - STERILEK250620KLS Martin Ixos System

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Related Devices (Code: JDQ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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