Nu Vasive, Incorporated
Nu Vasive, Incorporated holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2023.
Clearances by Nu Vasive, Incorporated — page 2
101–112 of 112- K140563 — LATERAL VBR SYSTEM
- K140479 — COROENT XL-F SYSTEM
- K140921 — COROENT SMALL INTERBODY SYSTEM
- K140770 — MLX - MEDIAL LATERAL EXPANDABLE LUMBAR INTERBODY SYSTEM
- K140659 — COROENT THORACOLUMBAR IMPLANTS
- K132694 — NUVASIVE NVM5 SYSTEM
- K133530 — NUVASIVE EMG ENDOTRACHEAL TUBE
- K132601 — COROENT STERILE IMPLANTS SYSTEM
- K132411 — AFFIX II SPINOUS PROCESS PLATE SYSTEM
- K130820 — EXPANDABLE LUMBAR INTERBODY SYSTEM
- K122910 — ARCHON ANTERIOR CERVICAL PLATE SYSTE,
- K112709 — STIMULATION/DISSECTION INSTRUMENTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.