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 |