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

Clearance record K100210

TRANS1 LATERAL INTERVERTEBRAL FUSION DEVICE, T · Trans1 Incorporated · decided 2010-08-26 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
VEOV070-61709CGChoice Spine, LPLXH00840996177184
VeoV070-A61709RChoice Spine, LPLXH00840996181365
VEOV070-A61707LChoice Spine, LPLXH00840996181303
VeoV070-A61715RChoice Spine, LPLXH00840996181396
VeoV070-A61709LChoice Spine, LPLXH00840996181310
VeoV070-A61711RChoice Spine, LPLXH00840996181389
VEOV070-61711CGChoice Spine, LPLXH00840996177191
VEOV070-61708CGChoice Spine, LPLXH00840996177177
VeoV070-A61713RChoice Spine, LPLXH00840996181372