2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES
K-Number: K102694 · 2010-12-09
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Device Summary
Frequently Asked Questions
What is the 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES?
2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES is a medical device that received FDA 510(k) clearance on 2010-12-09. The listed applicant is Synthes (Usa). The 510(k) number is K102694.
When did 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES receive FDA 510(k) clearance?
2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES received FDA 510(k) clearance on 2010-12-09, under 510(k) number K102694.
Who is the listed applicant for 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES?
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 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES?
The FDA product code for 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES 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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