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FDA 510(k)

MOUNTAINEER OCT SPINAL SYSTEM

K-Number: K132332 · 2013-08-22

Decision Date2013-08-22
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MOUNTAINEER OCT SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2013-08-22 under 510(k) number K132332. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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 2013-08-22. The listed applicant is Medos International SARL. The 510(k) number is K132332.

When did MOUNTAINEER OCT SPINAL SYSTEM receive FDA 510(k) clearance?

MOUNTAINEER OCT SPINAL SYSTEM received FDA 510(k) clearance on 2013-08-22, under 510(k) number K132332.

Who is the listed applicant for MOUNTAINEER OCT SPINAL SYSTEM?

The FDA 510(k) record lists Medos International SARL 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 Medos International SARL 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.

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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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