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FDA 510(k)

HAIG NAIL

K-Number: K940736 · 1994-09-12

ApplicantHowmedica Corp.
Decision Date1994-09-12
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HAIG NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1994-09-12 under 510(k) number K940736. 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 HAIG NAIL?

HAIG NAIL is a medical device that received FDA 510(k) clearance on 1994-09-12. The listed applicant is Howmedica Corp.. The 510(k) number is K940736.

When did HAIG NAIL receive FDA 510(k) clearance?

HAIG NAIL received FDA 510(k) clearance on 1994-09-12, under 510(k) number K940736.

Who is the listed applicant for HAIG NAIL?

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 HAIG NAIL?

The FDA product code for HAIG NAIL is JDS.

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

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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