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FDA 510(k)

HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST

K-Number: K864929 · 1987-01-28

ApplicantHall Surgical, Division of Zimmer, Inc.
Decision Date1987-01-28
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST 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 1987-01-28 under 510(k) number K864929. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST?

HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST is a medical device that received FDA 510(k) clearance on 1987-01-28. The listed applicant is Hall Surgical, Division of Zimmer, Inc.. The 510(k) number is K864929.

When did HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST receive FDA 510(k) clearance?

HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST received FDA 510(k) clearance on 1987-01-28, under 510(k) number K864929.

Who is the listed applicant for HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST?

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 (R) MICRO E POWERED SURGICAL INSTRUMENT SYST?

The FDA product code for HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYST is HWE.

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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 SYSTEMK864163HALL DUNBAR DRILL GUIDE SYSTEMK862778HALL CANNLULA SYSTEMK862474HALL STERNUM SAWK862529HALL STERILE BUR

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Related Devices (Code: HWE)

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.

K102743ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRESOrtho Solutions LimitedK063688SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBEThe Anspach Effort, Inc.K050766EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEMZimmer TrabecularK043310SYNTHES (USA) ELECTRIC PEN DRIVE SYSTEMSynthes (Usa)K022744REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSMedical Device ServicesK012694REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSAdven Medical

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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