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FDA 510(k)

KLS Martin Drill-Free MMF Screw

K-Number: K233721 · 2024-09-17

ApplicantKLS-Martin L.P.
Decision Date2024-09-17
Product CodeDZL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KLS Martin Drill-Free MMF Screw is a medical device manufactured by KLS-Martin L.P.. It received FDA 510(k) clearance on 2024-09-17 under approval number K233721. The device is classified under product code DZL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLS Martin Drill-Free MMF Screw?

KLS Martin Drill-Free MMF Screw is a medical device that received FDA 510(k) clearance on 2024-09-17. It is manufactured by KLS-Martin L.P.. The 510(k) number is K233721.

When was KLS Martin Drill-Free MMF Screw approved by the FDA?

KLS Martin Drill-Free MMF Screw received FDA 510(k) clearance on 2024-09-17, under approval number K233721.

What company makes KLS Martin Drill-Free MMF Screw?

KLS Martin Drill-Free MMF Screw is manufactured by KLS-Martin L.P..

What is the FDA product code for KLS Martin Drill-Free MMF Screw?

The FDA product code for KLS Martin Drill-Free MMF Screw is DZL.

Other Devices by KLS-Martin L.P.

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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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