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FDA 510(k)

Fortress™ Pedicular Fixation System

K-Number: K170268 · 2017-04-14

Decision Date2017-04-14
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Fortress™ Pedicular Fixation System is the device name listed in this FDA 510(k) record. The listed applicant is Spineology, Inc.. It received FDA 510(k) clearance on 2017-04-14 under 510(k) number K170268. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Fortress™ Pedicular Fixation System?

Fortress™ Pedicular Fixation System is a medical device that received FDA 510(k) clearance on 2017-04-14. The listed applicant is Spineology, Inc.. The 510(k) number is K170268.

When did Fortress™ Pedicular Fixation System receive FDA 510(k) clearance?

Fortress™ Pedicular Fixation System received FDA 510(k) clearance on 2017-04-14, under 510(k) number K170268.

Who is the listed applicant for Fortress™ Pedicular Fixation System?

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

What is the FDA product code for Fortress™ Pedicular Fixation System?

The FDA product code for Fortress™ Pedicular Fixation System is NKB.

Other records listing Spineology, 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.

View all 32 devices →

Related Devices (Code: NKB)

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

View on FDA Database →

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