LIFE SPINE LUMBAR PLATE SYSTEM
K-Number: K093200 · 2010-01-19
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Device Summary
Frequently Asked Questions
What is the LIFE SPINE LUMBAR PLATE SYSTEM?
LIFE SPINE LUMBAR PLATE SYSTEM is a medical device that received FDA 510(k) clearance on 2010-01-19. The listed applicant is Life Spine. The 510(k) number is K093200.
When did LIFE SPINE LUMBAR PLATE SYSTEM receive FDA 510(k) clearance?
LIFE SPINE LUMBAR PLATE SYSTEM received FDA 510(k) clearance on 2010-01-19, under 510(k) number K093200.
Who is the listed applicant for LIFE SPINE LUMBAR PLATE SYSTEM?
The FDA 510(k) record lists Life Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIFE SPINE LUMBAR PLATE SYSTEM?
The FDA product code for LIFE SPINE LUMBAR PLATE SYSTEM 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 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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