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FDA 510(k)

IMPLEX ALUMINA FEMORAL HEAD

K-Number: K990183 · 1999-06-11

ApplicantImplex Corp.
Decision Date1999-06-11
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IMPLEX ALUMINA FEMORAL HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Implex Corp.. It received FDA 510(k) clearance on 1999-06-11 under 510(k) number K990183. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLEX ALUMINA FEMORAL HEAD?

IMPLEX ALUMINA FEMORAL HEAD is a medical device that received FDA 510(k) clearance on 1999-06-11. The listed applicant is Implex Corp.. The 510(k) number is K990183.

When did IMPLEX ALUMINA FEMORAL HEAD receive FDA 510(k) clearance?

IMPLEX ALUMINA FEMORAL HEAD received FDA 510(k) clearance on 1999-06-11, under 510(k) number K990183.

Who is the listed applicant for IMPLEX ALUMINA FEMORAL HEAD?

The FDA 510(k) record lists Implex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLEX ALUMINA FEMORAL HEAD?

The FDA product code for IMPLEX ALUMINA FEMORAL HEAD is LZO.

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Other records listing Implex 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.

K051978TRABECULAR METAL VERTEBRAL BODY REPLACEMENTK051196TRABECULAR METAL VERTEBRAL BODY REPLACEMENT, MODEL 06-165-011X1 AND 06-166-051X1K040487TRABECULAR METAL KNEE SYSTEM AUGMENTSK040630TRABECULAR METAL FEMORAL CONE AUGMENTS, MODEL 03-125-ZZZZK040756THE TRABECULAR METAL RECONSTRUCTION SYSTEM, MODEL 10-340-XXXXXK031962NEXGEN TRABECULAR METAL TIBIAL CONE AUGMENTS

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Related Devices (Code: LZO)

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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