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FDA 510(k)

CANNULATED LAG SCREWS

K-Number: K863119 · 1986-09-03

ApplicantDowns Surgical , Ltd.
Decision Date1986-09-03
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CANNULATED LAG SCREWS 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 1986-09-03 under 510(k) number K863119. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULATED LAG SCREWS?

CANNULATED LAG SCREWS is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K863119.

When did CANNULATED LAG SCREWS receive FDA 510(k) clearance?

CANNULATED LAG SCREWS received FDA 510(k) clearance on 1986-09-03, under 510(k) number K863119.

Who is the listed applicant for CANNULATED LAG SCREWS?

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 CANNULATED LAG SCREWS?

The FDA product code for CANNULATED LAG SCREWS is HTY.

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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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