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FDA 510(k)

SEIDEL HUMERAL LOCKING NAIL

K-Number: K931256 · 1993-07-02

ApplicantHowmedica Corp.
Decision Date1993-07-02
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SEIDEL HUMERAL LOCKING NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K931256. 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 SEIDEL HUMERAL LOCKING NAIL?

SEIDEL HUMERAL LOCKING NAIL is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Howmedica Corp.. The 510(k) number is K931256.

When did SEIDEL HUMERAL LOCKING NAIL receive FDA 510(k) clearance?

SEIDEL HUMERAL LOCKING NAIL received FDA 510(k) clearance on 1993-07-02, under 510(k) number K931256.

Who is the listed applicant for SEIDEL HUMERAL LOCKING NAIL?

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 SEIDEL HUMERAL LOCKING NAIL?

The FDA product code for SEIDEL HUMERAL LOCKING NAIL 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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