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Captiva Spine, Inc

9 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers). recall (Z-1480-2015)Captiva Spine, Inc2015-04-21
CapLOX II Final Torque Driver, Indicator is a Pedicle screw spinal system. The CapLOX II S recall (Z-0413-2013)Captiva Spine, Inc2012-11-21
Accessories for the Captiva Spine FuseLOX Lumbar Cage. Products are labeled in part: "Fuse recall (Z-1783-2012)Captiva Spine, Inc2012-06-07
Accessories for the Captiva Spine FuseLOX Lumbar Cage. Products are labeled in part: "Fuse recall (Z-1784-2012)Captiva Spine, Inc2012-06-07
Accessories for the Captiva Spine FuseLOX Lumbar Cage. The Trial product is a reuseable co recall (Z-1785-2012)Captiva Spine, Inc2012-06-07
Accessories for the Captiva Spine FuseLOX Lumbar Cage. The FuseLOX Lumbar Inserter product recall (Z-1786-2012)Captiva Spine, Inc2012-06-07
Accessories for the Captiva Spine SmartLOX Cervical Plate System. Products are labeled in recall (Z-1648-2012)Captiva Spine, Inc2012-05-23
Accessories for the Captiva Spine SmartLOX Cervical Plate System. Products are labeled in recall (Z-1649-2012)Captiva Spine, Inc2012-05-23
Instructions For Use: "***SmartLOX***Instructions for Use Cervical Plate System***STERILIZ recall (Z-1545-2012)Captiva Spine, Inc2012-05-14

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Every clearance here is in the API, with alerts when new ones post.