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FDA 510(k)

FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM

K-Number: K803196 · 1981-02-09

ApplicantHowmedica Corp.
Decision Date1981-02-09
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1981-02-09 under 510(k) number K803196. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM?

FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM is a medical device that received FDA 510(k) clearance on 1981-02-09. The listed applicant is Howmedica Corp.. The 510(k) number is K803196.

When did FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM receive FDA 510(k) clearance?

FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM received FDA 510(k) clearance on 1981-02-09, under 510(k) number K803196.

Who is the listed applicant for FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM?

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 FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM?

The FDA product code for FLEXIBLE PIN S SHAPED INTRAMED. SYSTEM is HSB.

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Other records listing Howmedica Corp. as applicant

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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: HSB)

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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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