三麗美壓縮螺釘
K 號：K261241 · 2026-05-14
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器材摘要
TriMed Compression Screws is the device name listed in this FDA 510(k) record. The listed applicant is TriMed, Inc.. It received FDA 510(k) clearance on 2026-05-14 under 510(k) number K261241. 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.
常見問題
What is the TriMed Compression Screws?
TriMed Compression Screws is a medical device that received FDA 510(k) clearance on 2026-05-14. The listed applicant is TriMed, Inc.. The 510(k) number is K261241.
When did TriMed Compression Screws receive FDA 510(k) clearance?
TriMed Compression Screws received FDA 510(k) clearance on 2026-05-14, under 510(k) number K261241.
Who is the listed applicant for TriMed Compression Screws?
FDA 510(k) 記錄將 TriMed, Inc. 列為申請人。這並不單獨確立設備製造商。
What is the FDA product code for TriMed Compression Screws?
The FDA product code for TriMed Compression Screws is HWC. This falls under the Cardiovascular category.
相關臨床試驗
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其他以 TriMed, Inc. 為申請人之記錄
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
K262344大型壓縮螺釘K262032TriMed 非跨越式手部融合板 (NSFL-STD)；TriMed 非跨越式手部融合板 (NSFR-STD)；TriMed 非跨越式手部融合板 (NSFL-SHB)；TriMed 非跨越式手部融合板 (NSFR-SHB)K254002TriMed 適應性承重板 (VBEAL-13-7S)；TriMed 適應性承重板 (VBEAR-13-7S)；TriMed 適應性承重板 (VBEAL-14-7S)；TriMed 適應性承重板 (VBEAR-14-7S)；TriMed 適應性承重板 (VBEAL-16-7S)；TriMed 適應性承重板 (VBEAR-16-7S)K252061遠端 extremities 系統K251134RipCordK251945TriMed 全腕融合系統（全腕融合板）
相關器械（代碼：HWC）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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