Orthofix, Inc. · Class II · Cleared May 24, 2011
| K-number | K111183 |
| Device name | ASCENT POSTERIOR OCCIPITAL THORACIC (POCT) SYSTEM (TITANIUM & COBALT CHROME RODS) |
| Applicant | Orthofix, Inc. |
| Product code | KWP |
| Device class | Class II |
| Decision date | May 24, 2011 |
| Decision | Substantially Equivalent |
| Regulation | 888.3050 |
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