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FDA 510(k)

HALL STERNUM SAW

K-Number: K862474 · 1986-07-17

ApplicantHall Surgical, Division of Zimmer, Inc.
Decision Date1986-07-17
Product CodeDWH
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HALL STERNUM SAW 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 1986-07-17 under 510(k) number K862474. The device is classified under product code DWH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL STERNUM SAW?

HALL STERNUM SAW is a medical device that received FDA 510(k) clearance on 1986-07-17. The listed applicant is Hall Surgical, Division of Zimmer, Inc.. The 510(k) number is K862474.

When did HALL STERNUM SAW receive FDA 510(k) clearance?

HALL STERNUM SAW received FDA 510(k) clearance on 1986-07-17, under 510(k) number K862474.

Who is the listed applicant for HALL STERNUM SAW?

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 STERNUM SAW?

The FDA product code for HALL STERNUM SAW is DWH.

Related Clinical Trials

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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 SYSTEMK862529HALL STERILE BUR

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Related Devices (Code: DWH)

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.

K904352CODMAN COLLINS RADIOPARENT STERNAL BLADESCodman & Shurtleff, Inc.K850483MICRO-AIRE STERNUM SAW REPLACEMENT BLADESMicro-Aire Surgical Instruments, Inc.K830189CARDIOVASCULAR SAW BLADESTemp Medical Products, 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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