ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO)
K-Number: K132589 · 2013-10-08
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Device Summary
Frequently Asked Questions
What is the ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO)?
ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO) is a medical device that received FDA 510(k) clearance on 2013-10-08. The listed applicant is Life Spine, Inc.. The 510(k) number is K132589.
When did ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO) receive FDA 510(k) clearance?
ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO) received FDA 510(k) clearance on 2013-10-08, under 510(k) number K132589.
Who is the listed applicant for ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO)?
The FDA 510(k) record lists Life Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO)?
The FDA product code for ANTERIOR LUMBAR PLATE SYSTEM (PRESIDIO) is KWQ.
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 Life 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: KWQ)
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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