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FDA 510(k)

MOORE'S STRAIGHT & THOMPSON'S CURVED STEM PROSTHE.

K-Number: K864631 · 1986-12-18

Decision Date1986-12-18
Product Code
DecisionSubstantially Equivalent

Device Summary

MOORE'S STRAIGHT & THOMPSON'S CURVED STEM PROSTHE. 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 1986-12-18 under 510(k) number K864631. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOORE'S STRAIGHT & THOMPSON'S CURVED STEM PROSTHE.?

MOORE'S STRAIGHT & THOMPSON'S CURVED STEM PROSTHE. is a medical device that received FDA 510(k) clearance on 1986-12-18. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K864631.

When did MOORE'S STRAIGHT & THOMPSON'S CURVED STEM PROSTHE. receive FDA 510(k) clearance?

MOORE'S STRAIGHT & THOMPSON'S CURVED STEM PROSTHE. received FDA 510(k) clearance on 1986-12-18, under 510(k) number K864631.

Who is the listed applicant for MOORE'S STRAIGHT & THOMPSON'S CURVED STEM PROSTHE.?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Downs Surgical , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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