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FDA 510(k)

HOWMEDICA MIX-KIT II

K-Number: K792186 · 1979-12-05

ApplicantHowmedica Corp.
Decision Date1979-12-05
Product CodeJDZ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HOWMEDICA MIX-KIT II is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-12-05 under 510(k) number K792186. The device is classified under product code JDZ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOWMEDICA MIX-KIT II?

HOWMEDICA MIX-KIT II is a medical device that received FDA 510(k) clearance on 1979-12-05. The listed applicant is Howmedica Corp.. The 510(k) number is K792186.

When did HOWMEDICA MIX-KIT II receive FDA 510(k) clearance?

HOWMEDICA MIX-KIT II received FDA 510(k) clearance on 1979-12-05, under 510(k) number K792186.

Who is the listed applicant for HOWMEDICA MIX-KIT II?

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 HOWMEDICA MIX-KIT II?

The FDA product code for HOWMEDICA MIX-KIT II is JDZ.

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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: JDZ)

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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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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