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FDA 510(k)

JEWETT HIP NAIL

K-Number: K903251 · 1990-07-30

ApplicantOnyx Medical Corp.
Decision Date1990-07-30
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

JEWETT HIP NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Onyx Medical Corp.. It received FDA 510(k) clearance on 1990-07-30 under 510(k) number K903251. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JEWETT HIP NAIL?

JEWETT HIP NAIL is a medical device that received FDA 510(k) clearance on 1990-07-30. The listed applicant is Onyx Medical Corp.. The 510(k) number is K903251.

When did JEWETT HIP NAIL receive FDA 510(k) clearance?

JEWETT HIP NAIL received FDA 510(k) clearance on 1990-07-30, under 510(k) number K903251.

Who is the listed applicant for JEWETT HIP NAIL?

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

What is the FDA product code for JEWETT HIP NAIL?

The FDA product code for JEWETT HIP NAIL is KTT.

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Other records listing Onyx Medical Corp. as applicant

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Related Devices (Code: KTT)

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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