Palisade™ Pedicular Fixation System
K-Number: K170266 · 2017-04-14
Device Summary
Frequently Asked Questions
What is the Palisade™ Pedicular Fixation System?
Palisade™ 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 K170266.
When did Palisade™ Pedicular Fixation System receive FDA 510(k) clearance?
Palisade™ Pedicular Fixation System received FDA 510(k) clearance on 2017-04-14, under 510(k) number K170266.
Who is the listed applicant for Palisade™ 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 Palisade™ Pedicular Fixation System?
The FDA product code for Palisade™ 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.
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.