LEGEND POWER ADAPTER MODEL: 6475000
K-Number: K101168 · 2010-08-24
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Device Summary
Frequently Asked Questions
What is the LEGEND POWER ADAPTER MODEL: 6475000?
LEGEND POWER ADAPTER MODEL: 6475000 is a medical device that received FDA 510(k) clearance on 2010-08-24. The listed applicant is Medtronic Sofamor Danek. The 510(k) number is K101168.
When did LEGEND POWER ADAPTER MODEL: 6475000 receive FDA 510(k) clearance?
LEGEND POWER ADAPTER MODEL: 6475000 received FDA 510(k) clearance on 2010-08-24, under 510(k) number K101168.
Who is the listed applicant for LEGEND POWER ADAPTER MODEL: 6475000?
The FDA 510(k) record lists Medtronic Sofamor Danek as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEGEND POWER ADAPTER MODEL: 6475000?
The FDA product code for LEGEND POWER ADAPTER MODEL: 6475000 is HBB.
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 Medtronic Sofamor Danek 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: HBB)
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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