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FDA 510(k)

FLEXMEDICS NITINOL MAMMORY WIRE

K-Number: K870156 · 1987-02-24

ApplicantFlexmedics
Decision Date1987-02-24
Product Code
DecisionSubstantially Equivalent

Device Summary

FLEXMEDICS NITINOL MAMMORY WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Flexmedics. It received FDA 510(k) clearance on 1987-02-24 under 510(k) number K870156. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXMEDICS NITINOL MAMMORY WIRE?

FLEXMEDICS NITINOL MAMMORY WIRE is a medical device that received FDA 510(k) clearance on 1987-02-24. The listed applicant is Flexmedics. The 510(k) number is K870156.

When did FLEXMEDICS NITINOL MAMMORY WIRE receive FDA 510(k) clearance?

FLEXMEDICS NITINOL MAMMORY WIRE received FDA 510(k) clearance on 1987-02-24, under 510(k) number K870156.

Who is the listed applicant for FLEXMEDICS NITINOL MAMMORY WIRE?

The FDA 510(k) record lists Flexmedics 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 Flexmedics 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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