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FDA 510(k)

KLS Martin LINOS Wrist System

K-Number: K222624 · 2023-05-25

ApplicantKLS-Martin L.P.
Decision Date2023-05-25
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

KLS Martin LINOS Wrist System is a medical device manufactured by KLS-Martin L.P.. It received FDA 510(k) clearance on 2023-05-25 under approval number K222624. 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 LINOS Wrist System?

KLS Martin LINOS Wrist System is a medical device that received FDA 510(k) clearance on 2023-05-25. It is manufactured by KLS-Martin L.P.. The 510(k) number is K222624.

When was KLS Martin LINOS Wrist System approved by the FDA?

KLS Martin LINOS Wrist System received FDA 510(k) clearance on 2023-05-25, under approval number K222624.

What company makes KLS Martin LINOS Wrist System?

KLS Martin LINOS Wrist System is manufactured by KLS-Martin L.P..

What is the FDA product code for KLS Martin LINOS Wrist System?

The FDA product code for KLS Martin LINOS Wrist System is 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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