The following data is part of a premarket notification filed by Orthofix, Inc. with the FDA for Icon (tm) Modular Pedicle Screw System.
| Device ID | K111448 |
| 510k Number | K111448 |
| Device Name: | ICON (TM) MODULAR PEDICLE SCREW SYSTEM |
| Classification | Thoracolumbosacral Pedicle Screw System |
| 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 | NKB |
| Subsequent Product Code | KWQ |
| Subsequent Product Code | MNH |
| Subsequent Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-05-24 |
| Decision Date | 2012-02-16 |
| Summary: | summary |