The following data is part of a premarket notification filed by Stryker Spine with the FDA for Xia Spinal System, Xia 4.5 Spinal System.
Device ID | K060361 |
510k Number | K060361 |
Device Name: | XIA SPINAL SYSTEM, XIA 4.5 SPINAL SYSTEM |
Classification | Thoracolumbosacral Pedicle Screw System |
Applicant | STRYKER SPINE 2 PEARL COURT Allendale, NJ 07401 |
Contact | Simona Voic |
Correspondent | Simona Voic STRYKER SPINE 2 PEARL COURT Allendale, NJ 07401 |
Product Code | NKB |
Subsequent Product Code | KWP |
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 | 2006-02-13 |
Decision Date | 2006-03-06 |
Summary: | summary |