SpineSTAR Ablation Instrument (10|15, Long) STR-1015L

No FDA recalls on record, checked 22 Oct 2026.

Trade Name

SpineSTAR Ablation Instrument (10|15, Long)

Generic Name

Radio-frequency ablation system

Model / Ref / Catalog

STR-1015L

Primary DI / UDI-DI

00850696006004

FDA Product Code

GEI

GMDN Term

Radio-frequency ablation system

Device Class

Class II

Regulation Number

878.4400

GUDID distribution status

Not in Commercial Distribution

• Space Cpsxl Bone Cement

  Class II

  FDA 510(k) K061531 Active Cleared 30 Aug 2006

• Stabili Erx Bone Cement, Model 1135, Stabilit Vertebral Augmentation System (for Use W/ Stabilit Erx Bone Cement)

  Class II

  FDA 510(k) K090986 Active Cleared 30 Dec 2009

• Modification to Space Cpsxl Bone Cement

  Class II

  FDA 510(k) K072496 Active Cleared 5 Oct 2007

• Ablation Instrument, Model 1635; Ablation Multiplex Catheter, Model 1682

  Class II

  FDA 510(k) K091310 Active Cleared 11 Aug 2010

• Space 360 Delivery System

  Class II

  FDA 510(k) K070351 Active Cleared 29 Jun 2007