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FDA 510(k)

HIP FRACTURE STEM SYSTEM

K-Number: K883179 · 1988-09-22

ApplicantHowmedica Corp.
Decision Date1988-09-22
Product CodeKWL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HIP FRACTURE STEM 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 1988-09-22 under 510(k) number K883179. The device is classified under product code KWL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIP FRACTURE STEM SYSTEM?

HIP FRACTURE STEM SYSTEM is a medical device that received FDA 510(k) clearance on 1988-09-22. The listed applicant is Howmedica Corp.. The 510(k) number is K883179.

When did HIP FRACTURE STEM SYSTEM receive FDA 510(k) clearance?

HIP FRACTURE STEM SYSTEM received FDA 510(k) clearance on 1988-09-22, under 510(k) number K883179.

Who is the listed applicant for HIP FRACTURE STEM 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 HIP FRACTURE STEM SYSTEM?

The FDA product code for HIP FRACTURE STEM SYSTEM is KWL.

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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.

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Related Devices (Code: KWL)

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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