FDA 510(k) Applications for Medical Device Product Code: OBL (Cement, Bone, Pre-Formed, Modular, Polymeric, Vertebroplasty)

FDA 510(k) Applications for Medical Device Product Code "OBL"
(Cement, Bone, Pre-Formed, Modular, Polymeric, Vertebroplasty)

FDA 510(k) Number	Applicant	Device Name	Decision Date
K063606	SPINE WAVE, INC.	MODIFICATION TO STAXX FX SYSTEM	04/13/2007