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FDA 510(k)

T-HANDLE HEX WRENCH

K-Number: K903270 · 1990-07-30

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

Device Summary

T-HANDLE HEX WRENCH 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 K903270. The device is classified under product code LXH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-HANDLE HEX WRENCH?

T-HANDLE HEX WRENCH 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 K903270.

When did T-HANDLE HEX WRENCH receive FDA 510(k) clearance?

T-HANDLE HEX WRENCH received FDA 510(k) clearance on 1990-07-30, under 510(k) number K903270.

Who is the listed applicant for T-HANDLE HEX WRENCH?

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 T-HANDLE HEX WRENCH?

The FDA product code for T-HANDLE HEX WRENCH is LXH.

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Other records listing Onyx Medical 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.

K942022FACE-IT SHIELDK931690SPOON PLATEK934614MINI FRAGMENT PLATEK931692T-PLATEK931680CANNULATED CANCELLOUS SCREWK931684EPIPHYSIS PLATE

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Related Devices (Code: LXH)

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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