The following data is part of a premarket notification filed by Orthofix with the FDA for Firebird Spinal Fixation System, Phoenix Mis Spinal Fixation System.
Device ID | K122901 |
510k Number | K122901 |
Device Name: | FIREBIRD SPINAL FIXATION SYSTEM, PHOENIX MIS SPINAL FIXATION SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | ORTHOFIX 3451 PLANO PARKWAY Lewisville, TX 75056 |
Contact | Jacki Geren |
Correspondent | Jacki Geren ORTHOFIX 3451 PLANO PARKWAY Lewisville, TX 75056 |
Product Code | NKB |
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 | 2012-09-21 |
Decision Date | 2012-12-03 |
Summary: | summary |