Arthrex Beaming系统
K号: K262975 · 2026-09-25
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器械摘要
Arthrex Beaming System is the device name listed in this FDA 510(k) record. The listed applicant is Arthrex, Inc.. It received FDA 510(k) clearance on 2026-09-25 under 510(k) number K262975. The device is classified under product code HWC. It was reviewed by the OR advisory panel. Product code HWC falls under the category of Cardiovascular, which includes vascular grafts and cardiovascular implants. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Arthrex Beaming System?
Arthrex Beaming System is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Arthrex, Inc.. The 510(k) number is K262975.
When did Arthrex Beaming System receive FDA 510(k) clearance?
Arthrex Beaming System received FDA 510(k) clearance on 2026-09-25, under 510(k) number K262975.
Who is the listed applicant for Arthrex Beaming System?
The FDA 510(k) record lists Arthrex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Arthrex Beaming System?
The FDA product code for Arthrex Beaming System is HWC. This falls under the Cardiovascular category.
相关临床试验
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列明Arthrex, Inc.为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
相关器械（代码：HWC）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
K260995DynaNail Helix® Fixation SystemMedShape, Inc.K254280F.A.S.T ScrewSteps OrthoK261057ActivaScrew™ Cannulated COMBioretec, Ltd.K260106OsteoCoil™ GT Active Compression SystemFlower Orthopedics Corporation DBA Conventus Flower OrthopedK262344Large Compression ScrewsTriMed, Inc.K253858GFS - Sterile Screws and Top HatT.A.G. Medical Products Corporation, Ltd.
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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