CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM
K-Number: K102204 · 2010-11-15
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Device Summary
Frequently Asked Questions
What is the CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM?
CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM is a medical device that received FDA 510(k) clearance on 2010-11-15. The listed applicant is Choicespine, LP. The 510(k) number is K102204.
When did CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM receive FDA 510(k) clearance?
CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM received FDA 510(k) clearance on 2010-11-15, under 510(k) number K102204.
Who is the listed applicant for CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM?
The FDA 510(k) record lists Choicespine, LP as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CHOICE SPINE STARFIRE PEDICLE SCREW SYSTEM?
The FDA product code for CHOICE SPINE STARFIRE PEDICLE SCREW 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 Choicespine, LP 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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