Apollo Spine, Inc. · Class II · Cleared Jan 12, 2011
| K-number | K102121 |
| Device name | ECLIPSE VERTEBRAL SPACER SYSTEM-LUMBAR |
| Applicant | Apollo Spine, Inc. |
| Product code | OVD |
| Device class | Class II |
| Decision date | Jan 12, 2011 |
| Decision | Substantially Equivalent |
| Regulation | 888.3080 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov