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FDA 510(k)

External Fixation System

K-Number: K173883 · 2018-09-07

Decision Date2018-09-07
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

External Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Life Spine, Inc.. It received FDA 510(k) clearance on 2018-09-07 under 510(k) number K173883. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the External Fixation System?

External Fixation System is a medical device that received FDA 510(k) clearance on 2018-09-07. The listed applicant is Life Spine, Inc.. The 510(k) number is K173883.

When did External Fixation System receive FDA 510(k) clearance?

External Fixation System received FDA 510(k) clearance on 2018-09-07, under 510(k) number K173883.

Who is the listed applicant for External Fixation System?

The FDA 510(k) record lists Life Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for External Fixation System?

The FDA product code for External Fixation System is KTT.

Other records listing Life Spine, Inc. 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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Related Devices (Code: KTT)

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.

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.