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FDA 510(k)

HANSEN-STREET TYPE INTRAMEDULLARY NAIL

K-Number: K903256 · 1990-07-30

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

Device Summary

HANSEN-STREET TYPE INTRAMEDULLARY 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 K903256. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HANSEN-STREET TYPE INTRAMEDULLARY NAIL?

HANSEN-STREET TYPE INTRAMEDULLARY 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 K903256.

When did HANSEN-STREET TYPE INTRAMEDULLARY NAIL receive FDA 510(k) clearance?

HANSEN-STREET TYPE INTRAMEDULLARY NAIL received FDA 510(k) clearance on 1990-07-30, under 510(k) number K903256.

Who is the listed applicant for HANSEN-STREET TYPE INTRAMEDULLARY 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 HANSEN-STREET TYPE INTRAMEDULLARY NAIL?

The FDA product code for HANSEN-STREET TYPE INTRAMEDULLARY NAIL is HSB.

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Related Devices (Code: HSB)

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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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