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FDA 510(k)

HOWMEDICE BONE PLUG

K-Number: K951860 · 1995-05-16

ApplicantHowmedica Corp.
Decision Date1995-05-16
Product CodeLZN
Advisory CommitteeSU
DecisionSubstantially Equivalent for Some Indications

Device Summary

HOWMEDICE BONE PLUG is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1995-05-16 under 510(k) number K951860. The device is classified under product code LZN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the HOWMEDICE BONE PLUG?

HOWMEDICE BONE PLUG is a medical device that received FDA 510(k) clearance on 1995-05-16. The listed applicant is Howmedica Corp.. The 510(k) number is K951860.

When did HOWMEDICE BONE PLUG receive FDA 510(k) clearance?

HOWMEDICE BONE PLUG received FDA 510(k) clearance on 1995-05-16, under 510(k) number K951860.

Who is the listed applicant for HOWMEDICE BONE PLUG?

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 HOWMEDICE BONE PLUG?

The FDA product code for HOWMEDICE BONE PLUG is LZN.

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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: LZN)

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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