510(k) K150521
K150521 is an FDA 510(k) premarket notification submitted by Rti Surgical, Inc. Dba Rti Biologics for the device "Interbody Fusion (IBF)/Vertebral Body Replacement(VBR) System". The FDA issued a decision of Substantially Equivalent on May 15, 2015. The device falls under product code ODP (Intervertebral Fusion Device With Bone Graft, Cervical), a Class II device regulated under 21 CFR 888.3080. Rti Surgical, Inc. Dba Rti Biologics has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 15, 2015
- Date Received
- Mar 2, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Intervertebral Fusion Device With Bone Graft, Cervical
- Device Class
- Class II
- Regulation Number
- 888.3080
- Review Panel
- OR
- Submission Type
- 510(k)
Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft.