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FDA 510(k)

HOFFMAN HOOP DEVICE

K-Number: K810644 · 1981-03-24

ApplicantHowmedica Corp.
Decision Date1981-03-24
Product Code
DecisionSubstantially Equivalent

Device Summary

HOFFMAN HOOP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1981-03-24 under 510(k) number K810644. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOFFMAN HOOP DEVICE?

HOFFMAN HOOP DEVICE is a medical device that received FDA 510(k) clearance on 1981-03-24. The listed applicant is Howmedica Corp.. The 510(k) number is K810644.

When did HOFFMAN HOOP DEVICE receive FDA 510(k) clearance?

HOFFMAN HOOP DEVICE received FDA 510(k) clearance on 1981-03-24, under 510(k) number K810644.

Who is the listed applicant for HOFFMAN HOOP DEVICE?

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

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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

View all 373 devices →

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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