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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K132014

GSB GLOBAL SPINAL BALANCE SYSTEM · Nuvasive, Inc. · decided 2013-10-31 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ReLine16116585Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517586360
ReLine15460130Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517581112
ReLine16011180Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517552228
ReLine15160580Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517296788
ReLine15160430Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517296047
ReLine15160260Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517295293
ReLine15150490Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517293282
ReLine15160055Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517281487
ReLine15150055Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517279040
ReLine12255520Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517258632
ReLine12250260Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517253897
ReLine12155095Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517246967
ReLine10027530Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517243676
ReLine11260100Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517236654
ReLine11255185Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517235947
ReLine11080560Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517207944
ReLine11060115Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517206763
ReLine11060085Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517206701
ReLine11030535Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517184214
ReLine11028050Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517181527
ReLine11026595Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517179876
ReLine11026550Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517179487
ReLine11020595Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517171795
ReLine11019512Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517170262
ReLine11017565Nuvasive, Inc.KWP KWQ MNH MNI NKB00887517167835