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FDA 510(k)

ROC LUMBAR PLATING SYSTEM

K-Number: K050078 · 2005-02-18

Decision Date2005-02-18
Product CodeMNH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ROC LUMBAR PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Alphatec/Nexmed. It received FDA 510(k) clearance on 2005-02-18 under 510(k) number K050078. The device is classified under product code MNH. It was reviewed by the OR advisory panel. Product code MNH falls under the category of ENT, which includes ear, nose, and throat diagnostic and surgical devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROC LUMBAR PLATING SYSTEM?

ROC LUMBAR PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2005-02-18. The listed applicant is Alphatec/Nexmed. The 510(k) number is K050078.

When did ROC LUMBAR PLATING SYSTEM receive FDA 510(k) clearance?

ROC LUMBAR PLATING SYSTEM received FDA 510(k) clearance on 2005-02-18, under 510(k) number K050078.

Who is the listed applicant for ROC LUMBAR PLATING SYSTEM?

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

What is the FDA product code for ROC LUMBAR PLATING SYSTEM?

The FDA product code for ROC LUMBAR PLATING SYSTEM is MNH. This falls under the ENT category.

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 Alphatec/Nexmed 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.

View all 9 devices →

Related Devices (Code: MNH)

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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