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FDA 510(k)

B.G. FLEXIBLE NAIL SYSTEM

K-Number: K770130 · 1977-01-26

ApplicantHowmedica Corp.
Decision Date1977-01-26
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

B.G. FLEXIBLE NAIL 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 1977-01-26 under 510(k) number K770130. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the B.G. FLEXIBLE NAIL SYSTEM?

B.G. FLEXIBLE NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Howmedica Corp.. The 510(k) number is K770130.

When did B.G. FLEXIBLE NAIL SYSTEM receive FDA 510(k) clearance?

B.G. FLEXIBLE NAIL SYSTEM received FDA 510(k) clearance on 1977-01-26, under 510(k) number K770130.

Who is the listed applicant for B.G. FLEXIBLE NAIL 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 B.G. FLEXIBLE NAIL SYSTEM?

The FDA product code for B.G. FLEXIBLE NAIL SYSTEM is JDS.

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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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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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