Spinal USA
Spinal USA holds FDA 510(k) medical device clearances, first cleared 2006, most recent 2013.
Top product codes for Spinal USA
Recent clearances by Spinal USA
- K132029 — VAULT-C INTERVERTEBRAL BODY FUSION DEVICE
- K130863 — FACET SCREW SYSTEM
- K131343 — REFORM PEDICLE SCREW SYSTEM
- K130279 — REFORM PEDICLE SCREW SYSTEM
- K130445 — VAULT ALIF SYSTEM
- K122931 — S-LOK PSS SYSTEM
- K121172 — REFORM PEDICLE SCREW SYSTEM
- K112025 — SURE LOK MINI POSTERIOR CERVICAL/UPPER THORACIC SYSTEM
- K103369 — VAULT ALIF SYSTEM
- K092659 — SPINAL USA RCS ANTERIOR LUMBAR BUTRESS PLATE SYSTEM, MODEL 22-1001-25
- K092193 — SPINAL USA INTERBODY CAGES
- K092128 — MODIFICATION TO: PSS SYSTEM
- K091044 — SPINAL USA ANTERIOR LUMBAR PLATE SYSTEM
- K083118 — SPINAL USA ANTERIOR CERVICAL INTERBODY FUSION DEVICE
- K090033 — MODIFICATION TO: PSS SYSTEM
- K081196 — SPINAL USA VBR SYSTEM
- K080314 — SPINAL USA INTERBODY FUSION DEVICE
- K073240 — PSS SYSTEM
- K070922 — MODIFICATION TO SPINAL USA VBR SYSTEM
- K071438 — PSS SYSTEM
- K061752 — SPINAL USA VBR SYSTEM
- K060025 — SLIMPLICITY ANTERIOR CERVICAL PLATE SYSTEM
- K060132 — SPINAL USA CEMENT RESTRICTOR SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.