AXLE PEEK INTERSPINOUS FUSION SYSTEM
K-Number: K112592 · 2011-12-05
Advertisement
Device Summary
Frequently Asked Questions
What is the AXLE PEEK INTERSPINOUS FUSION SYSTEM?
AXLE PEEK INTERSPINOUS FUSION SYSTEM is a medical device that received FDA 510(k) clearance on 2011-12-05. The listed applicant is X-Spine Systems, Inc.. The 510(k) number is K112592.
When did AXLE PEEK INTERSPINOUS FUSION SYSTEM receive FDA 510(k) clearance?
AXLE PEEK INTERSPINOUS FUSION SYSTEM received FDA 510(k) clearance on 2011-12-05, under 510(k) number K112592.
Who is the listed applicant for AXLE PEEK INTERSPINOUS FUSION SYSTEM?
The FDA 510(k) record lists X-Spine Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AXLE PEEK INTERSPINOUS FUSION SYSTEM?
The FDA product code for AXLE PEEK INTERSPINOUS FUSION SYSTEM is KWP.
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 X-Spine Systems, 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: KWP)
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.
Advertisement