LANX SPINAL FIXATION SYSTEM
K-Number: K103091 · 2011-04-15
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Device Summary
Frequently Asked Questions
What is the LANX SPINAL FIXATION SYSTEM?
LANX SPINAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2011-04-15. The listed applicant is Lanx, Inc.. The 510(k) number is K103091.
When did LANX SPINAL FIXATION SYSTEM receive FDA 510(k) clearance?
LANX SPINAL FIXATION SYSTEM received FDA 510(k) clearance on 2011-04-15, under 510(k) number K103091.
Who is the listed applicant for LANX SPINAL FIXATION SYSTEM?
The FDA 510(k) record lists Lanx, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LANX SPINAL FIXATION SYSTEM?
The FDA product code for LANX SPINAL FIXATION 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 Lanx, 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.
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