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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 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 2024-09-17 under 510(k) 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. The listed applicant is KLS-Martin L.P.. The 510(k) number is K233721.

When did KLS Martin Drill-Free MMF Screw receive FDA 510(k) clearance?

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

Who is the listed applicant for KLS Martin Drill-Free MMF Screw?

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 Drill-Free MMF Screw?

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

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: DZL)

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.

K250123Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)Hager& Meisinger GmbHK251569Bone ScrewOsstem Implant Co., Ltd.K243190USTOMED Bone Fixation/Bone Augmentation Systems - PINUstomed Instrumente Ulrich Storz GmbH & Co. KGK233419GBR SystemProimtech Saglik Urunleri Anonim SirketiK240321MP Pin flat without thread (36BMP000020/MP20)Hager& Meisinger GmbHK231599Stryker MP, Mandible, HMMF and MMF AXS ScrewsStryker Leibinger GmbH & Co KG

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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