K152532 is an FDA 510(k) clearance for the AERO -C Cervical Cage System. This device is classified as a Intervertebral Fusion Device With Bone Graft, Cervical (Class II — Special Controls, product code ODP).
Submitted by Stryker Spine (Allendale, US). The FDA issued a Cleared decision on December 18, 2015, 106 days after receiving the submission on September 3, 2015.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3080. Intended To Stabilize Cervical Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft..
| 510(k) Number | K152532 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 03, 2015 |
| Decision Date | December 18, 2015 |
| Days to Decision | 106 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | ODP — Intervertebral Fusion Device With Bone Graft, Cervical |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 888.3080 |
| Definition | Intended To Stabilize Cervical Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft. |