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FDA 510(k)

MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM

K-Number: K961704 · 1996-07-26

ApplicantDentatus USA , Ltd.
Decision Date1996-07-26
Product CodeELS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Dentatus USA , Ltd.. It received FDA 510(k) clearance on 1996-07-26 under 510(k) number K961704. The device is classified under product code ELS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM?

MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM is a medical device that received FDA 510(k) clearance on 1996-07-26. The listed applicant is Dentatus USA , Ltd.. The 510(k) number is K961704.

When did MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM receive FDA 510(k) clearance?

MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM received FDA 510(k) clearance on 1996-07-26, under 510(k) number K961704.

Who is the listed applicant for MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM?

The FDA 510(k) record lists Dentatus USA , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM?

The FDA product code for MTI-MP TRANSITIONAL IMPLANTS AND MODULAR PROSTHETIC SYSTEM is ELS.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dentatus USA , Ltd. 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.

K042931TUF LINK SILICONE RELINERK031793DENTATUS OSCIOMATK980620DENTATUS MTI MODULAR TRANSITIONAL IMPLANTS AND PROSTHETIC SYSTEM

Related Devices (Code: ELS)

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.

K972985SPLINT ITJeneric/Pentron, Inc.K922673FLEXIBLE CERAMIC ROPES AND TAPES FOR BONDINGGlasspan, Inc.K834363ENDIX RADICULAR BIOCERAMIC PINC.B.S. Biotechnics, Inc.K811209JACOB WIRZ TRANSFIXATION PINColmed, Ltd.K801525ZEST ENDODONTIC STABILIZERZest Anchors, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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