The following data is part of a premarket notification filed by Orthofix Inc. with the FDA for Ascent Posterior Occipital Thoracic (poct) System (titanium & Cobalt Chrome Rods).
| Device ID | K111183 |
| 510k Number | K111183 |
| Device Name: | ASCENT POSTERIOR OCCIPITAL THORACIC (POCT) SYSTEM (TITANIUM & COBALT CHROME RODS) |
| Classification | Appliance, Fixation, Spinal Interlaminal |
| Applicant | ORTHOFIX INC. 3451 PLANO PARKWAY Lewisville, TX 75056 |
| Contact | Darla Chew |
| Correspondent | Darla Chew ORTHOFIX INC. 3451 PLANO PARKWAY Lewisville, TX 75056 |
| Product Code | KWP |
| CFR Regulation Number | 888.3050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-04-27 |
| Decision Date | 2011-05-24 |
| Summary: | summary |