SYNTHES ANTERIOR CSLP SYSTEM
K-Number: K000536 · 2000-03-15
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Device Summary
Frequently Asked Questions
What is the SYNTHES ANTERIOR CSLP SYSTEM?
SYNTHES ANTERIOR CSLP SYSTEM is a medical device that received FDA 510(k) clearance on 2000-03-15. The listed applicant is Synthes Spine. The 510(k) number is K000536.
When did SYNTHES ANTERIOR CSLP SYSTEM receive FDA 510(k) clearance?
SYNTHES ANTERIOR CSLP SYSTEM received FDA 510(k) clearance on 2000-03-15, under 510(k) number K000536.
Who is the listed applicant for SYNTHES ANTERIOR CSLP SYSTEM?
The FDA 510(k) record lists Synthes Spine as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHES ANTERIOR CSLP SYSTEM?
The FDA product code for SYNTHES ANTERIOR CSLP 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 Synthes 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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