ROC LUMBAR PLATING SYSTEM
K-Number: K090228 · 2009-04-29
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Device Summary
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 2009-04-29. The listed applicant is Alphatec Spine, Inc.. The 510(k) number is K090228.
When did ROC LUMBAR PLATING SYSTEM receive FDA 510(k) clearance?
ROC LUMBAR PLATING SYSTEM received FDA 510(k) clearance on 2009-04-29, under 510(k) number K090228.
Who is the listed applicant for ROC LUMBAR PLATING SYSTEM?
The FDA 510(k) record lists Alphatec Spine, Inc. 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 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: 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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