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FDA 510(k)

MODIFIED HUCKSTEP INTRAMEDULLARY NAIL

K-Number: K871947 · 1987-08-05

ApplicantDowns Surgical , Ltd.
Decision Date1987-08-05
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFIED HUCKSTEP INTRAMEDULLARY NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1987-08-05 under 510(k) number K871947. 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 MODIFIED HUCKSTEP INTRAMEDULLARY NAIL?

MODIFIED HUCKSTEP INTRAMEDULLARY NAIL is a medical device that received FDA 510(k) clearance on 1987-08-05. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K871947.

When did MODIFIED HUCKSTEP INTRAMEDULLARY NAIL receive FDA 510(k) clearance?

MODIFIED HUCKSTEP INTRAMEDULLARY NAIL received FDA 510(k) clearance on 1987-08-05, under 510(k) number K871947.

Who is the listed applicant for MODIFIED HUCKSTEP INTRAMEDULLARY NAIL?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED HUCKSTEP INTRAMEDULLARY NAIL?

The FDA product code for MODIFIED HUCKSTEP INTRAMEDULLARY 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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