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

Clearance record K173030

Vertera Spine Cohere Cervical Interbody Fusion Device · Nu Vasive, Incorporated · decided 2017-11-21 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Cohere4091427P2Nuvasive, Inc.ODP00195377006752
Cohere4101647P2Nuvasive, Inc.ODP00195377006691
Cohere4081427P2Nuvasive, Inc.ODP00195377006769
Cohere4061427P2Nuvasive, Inc.ODP00195377006813
Cohere4091647P2Nuvasive, Inc.ODP00195377006745
Cohere4081647P2Nuvasive, Inc.ODP00887517056368
Cohere4071647P2Nuvasive, Inc.ODP00195377006783
Cohere4101427P2Nuvasive, Inc.ODP00195377006707
Cohere4071427P2Nuvasive, Inc.ODP00195377006790
Cohere4061647P2Nuvasive, Inc.ODP00195377006806