Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Spinal USA

FDA 510(k) & PMA Approved Devices — 23 products

Total Devices23
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K132029 VAULT-C INTERVERTEBRAL BODY FUSION DEVICEOVE2013-11-25 View
510(k) K130863 FACET SCREW SYSTEMMRW2013-08-09 View
510(k) K131343 REFORM PEDICLE SCREW SYSTEMMNI2013-07-24 View
510(k) K130279 REFORM PEDICLE SCREW SYSTEMMNI2013-06-20 View
510(k) K130445 VAULT ALIF SYSTEMOVD2013-04-25 View
510(k) K122931 S-LOK PSS SYSTEMMNI2012-11-20 View
510(k) K121172 REFORM PEDICLE SCREW SYSTEMMNI2012-08-08 View
510(k) K112025 SURE LOK MINI POSTERIOR CERVICAL/UPPER THORACIC SYSTEMKWP2011-09-15 View
510(k) K103369 VAULT ALIF SYSTEMOVD2011-04-04 View
510(k) K092659 SPINAL USA RCS ANTERIOR LUMBAR BUTRESS PLATE SYSTEM, MODEL 22-1001-25KWQ2009-11-17 View
510(k) K092193 SPINAL USA INTERBODY CAGESMAX2009-09-25 View
510(k) K092128 MODIFICATION TO: PSS SYSTEMMNI2009-09-14 View
510(k) K091044 SPINAL USA ANTERIOR LUMBAR PLATE SYSTEMKWQ2009-07-09 View
510(k) K083118 SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICEODP2009-05-27 View
510(k) K090033 MODIFICATION TO: PSS SYSTEMMNI2009-05-06 View
510(k) K081196 SPINAL USA VBR SYSTEMMAX2008-10-16 View
510(k) K080314 SPINAL USA INTERBODY FUSION DEVICEMAX2008-05-13 View
510(k) K073240 PSS SYSTEMMNI2008-03-20 View
510(k) K070922 MODIFICATION TO SPINAL USA VBR SYSTEMKWQ2007-09-19 View
510(k) K071438 PSS SYSTEMMNI2007-08-21 View
↑