MOUNTAINEER OCT SPINAL SYSTEM
K-Number: K110353 · 2011-04-07
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Device Summary
Frequently Asked Questions
What is the MOUNTAINEER OCT SPINAL SYSTEM?
MOUNTAINEER OCT SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2011-04-07. The listed applicant is Depuy Spine, Inc.. The 510(k) number is K110353.
When did MOUNTAINEER OCT SPINAL SYSTEM receive FDA 510(k) clearance?
MOUNTAINEER OCT SPINAL SYSTEM received FDA 510(k) clearance on 2011-04-07, under 510(k) number K110353.
Who is the listed applicant for MOUNTAINEER OCT SPINAL SYSTEM?
The FDA 510(k) record lists Depuy Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOUNTAINEER OCT SPINAL SYSTEM?
The FDA product code for MOUNTAINEER OCT SPINAL 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 Depuy 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.
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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