LAPIDUS PLATE
K-Number: K060476 · 2006-05-17
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Device Summary
Frequently Asked Questions
What is the LAPIDUS PLATE?
LAPIDUS PLATE is a medical device that received FDA 510(k) clearance on 2006-05-17. The listed applicant is New Deal, S.A.. The 510(k) number is K060476.
When did LAPIDUS PLATE receive FDA 510(k) clearance?
LAPIDUS PLATE received FDA 510(k) clearance on 2006-05-17, under 510(k) number K060476.
Who is the listed applicant for LAPIDUS PLATE?
The FDA 510(k) record lists New Deal, S.A. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAPIDUS PLATE?
The FDA product code for LAPIDUS PLATE is HRS.
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 New Deal, S.A. 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: HRS)
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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