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FDA 510(k)

MINILINE BRACKET

K-Number: K881789 · 1988-06-01

ApplicantAlexotek Co.
Decision Date1988-06-01
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINILINE BRACKET is the device name listed in this FDA 510(k) record. The listed applicant is Alexotek Co.. It received FDA 510(k) clearance on 1988-06-01 under 510(k) number K881789. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINILINE BRACKET?

MINILINE BRACKET is a medical device that received FDA 510(k) clearance on 1988-06-01. The listed applicant is Alexotek Co.. The 510(k) number is K881789.

When did MINILINE BRACKET receive FDA 510(k) clearance?

MINILINE BRACKET received FDA 510(k) clearance on 1988-06-01, under 510(k) number K881789.

Who is the listed applicant for MINILINE BRACKET?

The FDA 510(k) record lists Alexotek Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINILINE BRACKET?

The FDA product code for MINILINE BRACKET is EJF.

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 Alexotek Co. 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.

K834446ALEXOTEK LINGUAL TUBESK834392LABIAL CUSPID TUBEK834272ALEXOLOK BRACKET

Related Devices (Code: EJF)

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.

K994357BITEM LOCK, MODELS SW006, SW012Thermoelastic Technologies, Inc.K932825MICROARCH GOLD BRACKETGac Intl., Inc.K933501ALASTIKUnitek Corp.K923372MEMORY WIREAlthan, Inc.K933080ORTHOTECH DURA-GOLD BARCKETSOrthotechK935139FASCINATION CERAMIC BRACKETDentauraum, 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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