SOLANAS AVALON POSTERIOR FIXATION SYSTEM
K-Number: K111076 · 2011-07-12
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Device Summary
Frequently Asked Questions
What is the SOLANAS AVALON POSTERIOR FIXATION SYSTEM?
SOLANAS AVALON POSTERIOR FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2011-07-12. The listed applicant is Alphatec Spine, Inc.. The 510(k) number is K111076.
When did SOLANAS AVALON POSTERIOR FIXATION SYSTEM receive FDA 510(k) clearance?
SOLANAS AVALON POSTERIOR FIXATION SYSTEM received FDA 510(k) clearance on 2011-07-12, under 510(k) number K111076.
Who is the listed applicant for SOLANAS AVALON POSTERIOR FIXATION 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 SOLANAS AVALON POSTERIOR FIXATION SYSTEM?
The FDA product code for SOLANAS AVALON POSTERIOR FIXATION SYSTEM is NKB.
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: NKB)
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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