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FDA 510(k)

HALL STERILE BUR

K-Number: K862529 · 1986-07-15

ApplicantHall Surgical, Division of Zimmer, Inc.
Decision Date1986-07-15
Product CodeHTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HALL STERILE BUR is the device name listed in this FDA 510(k) record. The listed applicant is Hall Surgical, Division of Zimmer, Inc.. It received FDA 510(k) clearance on 1986-07-15 under 510(k) number K862529. The device is classified under product code HTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL STERILE BUR?

HALL STERILE BUR is a medical device that received FDA 510(k) clearance on 1986-07-15. The listed applicant is Hall Surgical, Division of Zimmer, Inc.. The 510(k) number is K862529.

When did HALL STERILE BUR receive FDA 510(k) clearance?

HALL STERILE BUR received FDA 510(k) clearance on 1986-07-15, under 510(k) number K862529.

Who is the listed applicant for HALL STERILE BUR?

The FDA 510(k) record lists Hall Surgical, Division of Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HALL STERILE BUR?

The FDA product code for HALL STERILE BUR is HTT.

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.

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Other records listing Hall Surgical, Division of Zimmer, Inc. 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.

K942660HALL MICROCHOICE ELECTRIC POWERED SYSTEMK864734HALL ORAL IMPLANT SYSTEMK864929HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYSTK864163HALL DUNBAR DRILL GUIDE SYSTEMK862778HALL CANNLULA SYSTEMK862474HALL STERNUM SAW

View all 8 devices →

Related Devices (Code: HTT)

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.

K821695MICRO-AIRE REPLAC. DRILL BURS FOR ZIMMERMicro-Aire Surgical Instruments, Inc.K802598CARBIDE CUTTING INSTRUMENT/INTRAARTICUThe Anspach Effort, Inc.K760236BUR, SURGICAL CARBIDECutter Laboratories, Inc.

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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