Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IMPLANT DRIVERS AND TIPS

K-Number: K781974 · 1978-12-28

ApplicantMiter, Inc.
Decision Date1978-12-28
Product CodeDZJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLANT DRIVERS AND TIPS is the device name listed in this FDA 510(k) record. The listed applicant is Miter, Inc.. It received FDA 510(k) clearance on 1978-12-28 under 510(k) number K781974. The device is classified under product code DZJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANT DRIVERS AND TIPS?

IMPLANT DRIVERS AND TIPS is a medical device that received FDA 510(k) clearance on 1978-12-28. The listed applicant is Miter, Inc.. The 510(k) number is K781974.

When did IMPLANT DRIVERS AND TIPS receive FDA 510(k) clearance?

IMPLANT DRIVERS AND TIPS received FDA 510(k) clearance on 1978-12-28, under 510(k) number K781974.

Who is the listed applicant for IMPLANT DRIVERS AND TIPS?

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

What is the FDA product code for IMPLANT DRIVERS AND TIPS?

The FDA product code for IMPLANT DRIVERS AND TIPS is DZJ.

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

Related Devices (Code: DZJ)

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.

K261826VSP System (Titanium Palatal Splint)3D Systems, Inc.K243637Materialise Personalized Guides and Models for Craniomaxillofacial SurgeryMaterialise NVK242263TECHFIT DISRP® SystemTechfit Digital Surgery, Inc.K231520tmCMF SolutionTechmah CmfK230276TECHFIT DISRP® SystemTechfit Digital SurgeryK223024MedCAD AccuPlan SystemMedcad

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.

↑