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FDA 510(k)

ELLISON VITALLIUM FIXATION STAPLE SYS

K-Number: K822943 · 1982-10-27

ApplicantHowmedica Corp.
Decision Date1982-10-27
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ELLISON VITALLIUM FIXATION STAPLE SYS is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1982-10-27 under 510(k) number K822943. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELLISON VITALLIUM FIXATION STAPLE SYS?

ELLISON VITALLIUM FIXATION STAPLE SYS is a medical device that received FDA 510(k) clearance on 1982-10-27. The listed applicant is Howmedica Corp.. The 510(k) number is K822943.

When did ELLISON VITALLIUM FIXATION STAPLE SYS receive FDA 510(k) clearance?

ELLISON VITALLIUM FIXATION STAPLE SYS received FDA 510(k) clearance on 1982-10-27, under 510(k) number K822943.

Who is the listed applicant for ELLISON VITALLIUM FIXATION STAPLE SYS?

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

What is the FDA product code for ELLISON VITALLIUM FIXATION STAPLE SYS?

The FDA product code for ELLISON VITALLIUM FIXATION STAPLE SYS is JDR.

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Other records listing Howmedica Corp. as applicant

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Related Devices (Code: JDR)

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.

K262451Arthrex DynaNite StaplesArthrex, Inc.K261121Megalodon Dynamic Compression SystemParagon 28, Inc.K250712Linkt Compression Staple SystemTrax SurgicalK243888Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemMedline Industries, LPK243742Arthrex DynaNite Nitinol StaplesArthrex, Inc.K243658TMC Compression Implant SystemTreace Medical Concepts

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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