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FDA 510(k)

DALL-MILES HOMOGENOUS VITALLIUM CABLE

K-Number: K961283 · 1996-05-22

ApplicantHowmedica Corp.
Decision Date1996-05-22
Product CodeJDQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DALL-MILES HOMOGENOUS VITALLIUM CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1996-05-22 under 510(k) number K961283. The device is classified under product code JDQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DALL-MILES HOMOGENOUS VITALLIUM CABLE?

DALL-MILES HOMOGENOUS VITALLIUM CABLE is a medical device that received FDA 510(k) clearance on 1996-05-22. The listed applicant is Howmedica Corp.. The 510(k) number is K961283.

When did DALL-MILES HOMOGENOUS VITALLIUM CABLE receive FDA 510(k) clearance?

DALL-MILES HOMOGENOUS VITALLIUM CABLE received FDA 510(k) clearance on 1996-05-22, under 510(k) number K961283.

Who is the listed applicant for DALL-MILES HOMOGENOUS VITALLIUM CABLE?

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 DALL-MILES HOMOGENOUS VITALLIUM CABLE?

The FDA product code for DALL-MILES HOMOGENOUS VITALLIUM CABLE is JDQ.

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Other records listing Howmedica Corp. 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.

K983528MICRO DYNAMIC MESHK983404TYPE 3 FEMORAL COMPONENTSK980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATIONK980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATIONK980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATIONK980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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Related Devices (Code: JDQ)

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.

K261271Cable-Ready® Cable Grip SystemPioneer Surgical Technology, Inc.K243905Stitch Cerclage – Suture TapesGM Dos Reis Industria e Comercio Ltda.K243344Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape Cerclage SuturesArthrex, Inc.K232733Mbrace CableMedacta International S.A.K233949ACCORD Cable SystemSmith & Nephew, Inc.K232986VariTrax Sternal CircumFixation SystemCircumfix Solutions, 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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