Spineart
Spineart holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2023.
Top product codes for Spineart
Recent clearances by Spineart
- K230774 — PERLA® TL System; TEKTONA® HV US Bone Cement
- K213470 — PERLA® TL Posterior Osteosynthesis System
- K210472 — SPINEART Navigation Instrument System
- K203506 — PERLA® TL posterior osteosynthesis system
- K203222 — PERLA TL Posterior Osteosynthesis System
- K200571 — PERLA® Posterior Occipito-Cervico-Thoracic Fixation System
- K200312 — Tryptik Ti
- K193396 — PERLA® TL posterior osteosynthesis system
- K192993 — SCARLET AL-T
- K190877 — Juliet® Ti LL Lumbar Interbody Device
- K190322 — SCARLET® AC-T Secured Anterior Cervical Cage
- K190071 — Perla® Posterior Cervico-Thoracic Fixation System
- K181818 — Scarlet AL-T
- K181203 — Juliet Ti
- K171797 — TRYPTIK2 C-Plate Anterior Cervical Plate System
- K173702 — Juliet Ti LL
- K172065 — SCARLET AC-T
- K172101 — ROMEO® 2 Posterior Osteosynthesis System
- K161888 — JULIET® LL Lateral Lumbar Cage
- K153621 — Juliet® Ti
- K153042 — TRYPTIK2C-plate Anterior Cervical Plate System
- K153386 — Perla Posterior Cervico-Thoracic Fixation system
- K151104 — OTELO LL
- K151695 — Romeo posterior osteosynthesis system
- K143214 — SCARLET® AC-T Secured Anterior Cervical Cage
- K141135 — JULIET LL
- K142277 — JULIET PO
- K141314 — SCARLET AC-T SECURED ANTERIOR CERVICAL CAGE AND ASSOCIATED INSTRUMENTATION
- K141835 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM PREBENT CROSS-CONNECTORS; PREBENT RODS
- K141508 — ROMEO 2 PAD POSTERIOR AXIAL DEVICE
- K140948 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
- K140474 — JULIET OL
- K133557 — JULIET LL LATERAL LUMBAR CAGE
- K130267 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
- K122366 — TRYPTIK CC ANTERIOR INTERSOMATIC CERVICAL CAGE
- K112108 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
- K111127 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
- K101678 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
- K101720 — JULIET OL
- K093936 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
- K093170 — ROMEO POSTERIOR OSTEOSYNTHESIS SYSTEM
- K091873 — TRYPTIK CA ANTERIOR INTERSOMATIC CERVICAL CAGE, MODELS MOS-CA 12 05-S, MOS-CA 12 O6-S
- K081888 — DYNAMIK INTERVERTEBRAL BODY FUSION DEVICE
- K081165 — ELLIPSE LUMBAR POSTERIOR OSTEOSYNTHESIS SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.