SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG
K-Number: K041860 · 2004-09-08
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Device Summary
Frequently Asked Questions
What is the SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG?
SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG is a medical device that received FDA 510(k) clearance on 2004-09-08. The listed applicant is Synthes (Usa). The 510(k) number is K041860.
When did SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG receive FDA 510(k) clearance?
SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG received FDA 510(k) clearance on 2004-09-08, under 510(k) number K041860.
Who is the listed applicant for SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG?
The FDA 510(k) record lists Synthes (Usa) as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG?
The FDA product code for SYNTHES (USA) LCP PROXIMAL HUMERUS PLATES, LONG 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 Synthes (Usa) 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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