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FDA 510(k)

BONE DRILLS OR TAPS

K-Number: K914714 · 1993-11-15

ApplicantImplant Corp. of America
Decision Date1993-11-15
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BONE DRILLS OR TAPS is the device name listed in this FDA 510(k) record. The listed applicant is Implant Corp. of America. It received FDA 510(k) clearance on 1993-11-15 under 510(k) number K914714. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE DRILLS OR TAPS?

BONE DRILLS OR TAPS is a medical device that received FDA 510(k) clearance on 1993-11-15. The listed applicant is Implant Corp. of America. The 510(k) number is K914714.

When did BONE DRILLS OR TAPS receive FDA 510(k) clearance?

BONE DRILLS OR TAPS received FDA 510(k) clearance on 1993-11-15, under 510(k) number K914714.

Who is the listed applicant for BONE DRILLS OR TAPS?

The FDA 510(k) record lists Implant Corp. of America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BONE DRILLS OR TAPS?

The FDA product code for BONE DRILLS OR TAPS is DZE.

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 Implant Corp. of America 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.

K914715PARALLELING GUIDESK914724ADA SHANK EXTENSION

Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, 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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