Lanx, LLC
Lanx, LLC holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2012.
Top product codes for Lanx, LLC
Recent clearances by Lanx, LLC
- K120399 — LANX SPINAL FIXATION SYSTEM
- K102738 — LANX FUSION SYSTEM
- K103040 — LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
- K093285 — MODIFICATION TO LANX SPINAL FIXATION SYSTEM
- K082774 — LANX CERVICAL INTERVERTEBRAL BODY FUSION DEVICE
- K073144 — LANX INTERVERTEBRAL BODY FUSION DEVICE
- K071905 — POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM (PCFS)
- K071877 — LANX SPINAL FIXATION SYSTEM
- K071633 — LANX DEFORMITY SYSTEM
- K052384 — LANX VBR SYSTEM
- K043484 — LANX SPINAL FIXATION SYSTEM
- K050774 — LANX ANTERIOR CERVICAL PLATE SYSTEM
- K040401 — LANX ANTERIOR CERVIAL PLATE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.