免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据，仅供一般参考，不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Vitoss® 双模态生物活性骨移植替代泡沫条；Vitoss® 双模态生物活性骨移植替代品；Vitoss BBTrauma® 生物活性骨移植替代品；Vitoss® BA2X 生物活性骨移植替代品；Vitoss® 生物活性泡沫骨移植替代品套装；Vitoss® 生物活性泡沫骨移植替代品；Vitoss® 泡沫骨移植替代品；Vitoss® 骨移植替代品填充罐；Vitoss® 骨移植替代品

K号: K261008 · 2026-04-24

申请人Stryker Spine
决定日期2026-04-24
产品代码MQV
咨询委员会OR 请注意，由于原文中未提供具体的医疗设备监管文本，以下是一个示例翻译，您可以根据实际文本进行调整： --- 产品名称：[产品名称] 公司名称：[公司名称] 根据FDA 510(k)预市场批准程序，[产品名称]已获得批准，用于[产品用途描述]。 产品注册号：[注册号] PMA编号：[PMA编号] 临床试验编号（NCT）：[NCT编号] PubMed ID（PMID）：[PMID编号] 更多信息请访问以下链接： [URL] --- 请将上述示例中的[产品名称]、[公司名称]、[注册号]、[PMA编号]、[NCT编号]、[PMID编号]和[URL]替换为实际的文本内容。
决定实质等同

器械摘要

Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Spine. It received FDA 510(k) clearance on 2026-04-24 under 510(k) number K261008. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute?

Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute is a medical device that received FDA 510(k) clearance on 2026-04-24. The listed applicant is Stryker Spine. The 510(k) number is K261008.

When did Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute receive FDA 510(k) clearance?

Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute received FDA 510(k) clearance on 2026-04-24, under 510(k) number K261008.

Who is the listed applicant for Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute?

FDA 510(k)记录显示Stryker Spine为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute?

The FDA product code for Vitoss® BiModal Bioactive Bone Graft Substitute Foam Strip; Vitoss® BiModal Bioactive Bone Graft Substitute; Vitoss BBTrauma® Bioactive Bone Graft Substitute; Vitoss® BA2X Bioactive Bone Graft Substitute; Vitoss® Bioactive Foam Bone Graft Substitute Pack; Vitoss® Bioactive Foam Bone Graft Substitute; Vitoss® Foam Bone Graft Substitute; Vitoss® Bone Graft Substitute Filled Canister; Vitoss® Bone Graft Substitute is MQV.

相关临床试验

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

列明Stryker Spine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。

K262061Tritanium® C 前颈椎笼；Tritanium® PL笼；Tritanium® TL弯曲腰椎笼；Aero® -C 颈椎笼系统；AVS® Anchor-C 颈椎笼系统；AVS® TL PEEK间隔器；AVS® PL PEEK间隔器；AVS® 导航PEEK间隔器；AVS® AS PEEK间隔器；Monterey™ AL椎间系统；Aleutian IBF系统；Cascadia椎间系统；Chesapeake稳定系统；Sahara稳定系统；SANTORINI™ 脱位椎体笼系统；MOJAVE椎间系统；VLIFT VERTEBRAL BODY REPLACEMK242361OZARK 颈椎板系统；PYRENEES® 颈椎板系统；EVEREST® 脊柱系统；MESA® 脊柱系统；MESA® 小体型脊柱系统；CASPIAN® 脊柱系统；DENALI® 脊柱系统；DENALI® MI 脊柱系统；YUKON OCT 脊柱系统；Xia® 3 脊柱系统；K2M 病人专用；CASCADIA™ 椎间系统；CAYMAN® 板系统；CAYMAN® 板系统-MIK242280Vitoss® 双模态生物活性骨移植替代泡沫条，Vitoss® 双模态生物活性骨移植替代品，Vitoss BBTrauma® 生物活性骨移植替代品，Vitoss® BA2X 生物活性骨移植替代品，Vitoss® 生物活性骨移植替代品套装，Vitoss® 生物活性骨移植替代品，Vitoss® 泡沫骨移植替代品，Vitoss® 骨移植替代品填充罐，Vitoss® 骨移植替代品，Vitoss® 骨移植替代品 - 合成多孔片K222684XIA® 4.5 脊柱系统，XIA® 4.5 皮层轨迹，XIA® 3 脊柱系统，Serrato® 脊柱系统，XIA® 成长棒转换套件，XIA® II 脊柱系统，XIA® 精准系统，XIA® 前部，Diapason® 脊柱系统，Opus™ 脊柱系统，Radius® 脊柱系统，Mantis® 脊柱系统，Mantis® Redux，Trio® & Trio+ 脊柱固定系统，ES2™ 脊柱系统，ES2™ 可扩展脊柱系统，Oasys® 枕颈胸系统，Nile® 近端固定脊柱系统，Nile® 替代固定脊柱系统K221490Tritanium C 前颈椎笼，Tritanium PL笼，Tritanium TL弯曲后腰椎笼，Tritanium X PL可扩张后腰椎笼，Tritanium X TL可扩张弯曲后腰椎笼，Stryker Spine VLIFT 脊椎体置换系统，VLIFT-s 脊椎体置换系统，Ascential IBD PEEKc 间隔器，Aero-AL 腰椎笼系统，Aero-LL 腰椎笼系统，Aero-C 颈椎笼系统，AVS Aria PEEK 间隔器，AVS Anchor-C 颈椎笼系统，AVS Anchor-L 间隔器K203205导航脊柱器械

查看所有 13 个设备 →

相关器械（代码：MQV）

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。

K262230Mg OSTEOREVIVE™；Mg OSTEOCRETE™Bone Solutions, Inc.K260364设备300419条带Geistlich Pharma AGK252797JAZBI®可吸收骨空隙填充剂Sdip Innovations Pty, Ltd.K253524Adaptos®Fuse Bone GraftBiomendex OYK253147FIBERGRAFT™ BG Putty GPS Bone Graft Substitute FIBERGRAFT™ BG Putty Bone Graft Substitute FIBERGRAFT™ AERIDYAN™ Matrix Bone Graft Substitute FIBERGRAFT™ BG Matrix Bone Graft SubstituteProsidyan, Inc.K251522Mg OSTEOINJECT™；Mg OSTEOREVIVE™；Mg OSTEOCRETE™Bone Solutions, Inc.

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。

↑