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FDA 510(k)

ALTUS SPINE PEDICLE SCREW SYSTEM

K-Number: K132280 · 2013-10-31

Decision Date2013-10-31
Product CodeMNI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALTUS SPINE PEDICLE SCREW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Altus Partners. It received FDA 510(k) clearance on 2013-10-31 under 510(k) number K132280. The device is classified under product code MNI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTUS SPINE PEDICLE SCREW SYSTEM?

ALTUS SPINE PEDICLE SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2013-10-31. The listed applicant is Altus Partners. The 510(k) number is K132280.

When did ALTUS SPINE PEDICLE SCREW SYSTEM receive FDA 510(k) clearance?

ALTUS SPINE PEDICLE SCREW SYSTEM received FDA 510(k) clearance on 2013-10-31, under 510(k) number K132280.

Who is the listed applicant for ALTUS SPINE PEDICLE SCREW SYSTEM?

The FDA 510(k) record lists Altus Partners as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALTUS SPINE PEDICLE SCREW SYSTEM?

The FDA product code for ALTUS SPINE PEDICLE SCREW SYSTEM is MNI.

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.

Related Devices (Code: MNI)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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