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FDA 510(k)

POSTERIOR CRUCIATE CONDYLAR TIBIAL

K-Number: K790350 · 1979-03-06

ApplicantHowmedica Corp.
Decision Date1979-03-06
Product CodeHRY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

POSTERIOR CRUCIATE CONDYLAR TIBIAL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1979-03-06 under 510(k) number K790350. The device is classified under product code HRY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POSTERIOR CRUCIATE CONDYLAR TIBIAL?

POSTERIOR CRUCIATE CONDYLAR TIBIAL is a medical device that received FDA 510(k) clearance on 1979-03-06. The listed applicant is Howmedica Corp.. The 510(k) number is K790350.

When did POSTERIOR CRUCIATE CONDYLAR TIBIAL receive FDA 510(k) clearance?

POSTERIOR CRUCIATE CONDYLAR TIBIAL received FDA 510(k) clearance on 1979-03-06, under 510(k) number K790350.

Who is the listed applicant for POSTERIOR CRUCIATE CONDYLAR TIBIAL?

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 POSTERIOR CRUCIATE CONDYLAR TIBIAL?

The FDA product code for POSTERIOR CRUCIATE CONDYLAR TIBIAL is HRY.

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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: HRY)

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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