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FDA 510(k)

WOUND SPAN BRIDGE III

K-Number: K781837 · 1978-11-15

ApplicantHowmedica Corp.
Decision Date1978-11-15
Product CodeKAS
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

WOUND SPAN BRIDGE III is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1978-11-15 under 510(k) number K781837. The device is classified under product code KAS. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOUND SPAN BRIDGE III?

WOUND SPAN BRIDGE III is a medical device that received FDA 510(k) clearance on 1978-11-15. The listed applicant is Howmedica Corp.. The 510(k) number is K781837.

When did WOUND SPAN BRIDGE III receive FDA 510(k) clearance?

WOUND SPAN BRIDGE III received FDA 510(k) clearance on 1978-11-15, under 510(k) number K781837.

Who is the listed applicant for WOUND SPAN BRIDGE III?

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 WOUND SPAN BRIDGE III?

The FDA product code for WOUND SPAN BRIDGE III is KAS.

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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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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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