Camber Spine Technologies
Camber Spine Technologies holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2024.
Top product codes for Camber Spine Technologies
Recent clearances by Camber Spine Technologies
- K234077 — SPIRA® Anterior Lumbar Spacers
- K233972 — Camber Sacroiliac (SI) Fixation System
- K230942 — SPIRA® Posterior Lumbar Spacers
- K221324 — ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)
- K223837 — SPIRA®-C Integrated Fixation System
- K220038 — Camber Spine Navigation System
- K193153 — SPIRA-C Integrated Fixation System
- K190483 — SPIRA Open Matrix ALIF and LLIF
- K173432 — ENZA-A Titanium ALIF
- K173800 — Camber Spine Technologies SPIRA - V Open Matrix Corpectomy Cage
- K172446 — SPIRA-C Open Matrix Cervical Interbody
- K172064 — Ti-Diagon Oblique TLIF
- K170550 — Coveris Cervical Cage System
- K162986 — SPIRA Open Matrix ALIF
- K162121 — Siconus SI Joint Fixation System
- K153720 — ENZA Zero-Profile Anterior Interbody Fusion
- K121254 — CAMBER SPINE TECHNOLOGIES TLS 5.0 INERBODY CAGE
Data sourced from openFDA. This site is unofficial and independent of the FDA.