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FDA 510(k)

WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW

K-Number: K993603 · 1999-11-19

ApplicantHowmedica Osteonics Corp.
Decision Date1999-11-19
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 1999-11-19 under 510(k) number K993603. 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 WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW?

WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW is a medical device that received FDA 510(k) clearance on 1999-11-19. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K993603.

When did WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW receive FDA 510(k) clearance?

WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW received FDA 510(k) clearance on 1999-11-19, under 510(k) number K993603.

Who is the listed applicant for WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW?

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

What is the FDA product code for WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW?

The FDA product code for WICHITA FUSION NAIL FULLY THREADED SELF-TAPPING SCREW is 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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