Spine Vision, Inc.
Spine Vision, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2005.
Top product codes for Spine Vision, Inc.
Recent clearances by Spine Vision, Inc.
- K052406 — UNI-THREAD SPINAL SYSTEM
- K030526 — PEDIGUARD NERVE DETECTOR SYSTEM
- K042930 — SPACEVISION CAGE SYSTEM
- K042640 — UNI-THREAD SPINAL SYSTEM
- K033508 — PLUS PIVOT LINK UNIVERSAL SYSTEM
- K032398 — PLUS PIVOT LINK UNIVERSAL SYSTEM
- K022271 — PLUS PIVOT LINK UNIVERSAL SYSTEM
- K021507 — PLUS PIVOT LINK UNIVERSAL SYSTEM
- K021510 — UNI-T UNI-THREAD SPINAL SYSTEM
- K013301 — UNI-T SPINAL SYSTEM
- K013312 — P.L.U.S. SYSTEM (PIVOT LINK UNIVERSAL SYSTEM)
- K012881 — C3 ANTERIOR CERVICAL PLATE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.