The following data is part of a premarket notification filed by Orthofix Inc. with the FDA for Firebird Spinal Fixation System, Phoenix Mis Spinal Fixation System, Janus Midline Fixation Screw, Phoenix Cdx Mis Spinal Fixation System, Firebird Nxg Spinal Fixation System.
Device ID | K171082 |
510k Number | K171082 |
Device Name: | Firebird Spinal Fixation System, Phoenix MIS Spinal Fixation System, JANUS Midline Fixation Screw, Phoenix CDX MIS Spinal Fixation System, Firebird NXG Spinal Fixation System |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Contact | Jacki Koch |
Correspondent | Jacki Koch Orthofix Inc. 3451 Plano Parkway Lewisville, TX 75056 |
Product Code | NKB |
Subsequent Product Code | KWP |
Subsequent Product Code | KWQ |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-04-11 |
Decision Date | 2017-05-05 |
Summary: | summary |