The following data is part of a premarket notification filed by X-spine Systems, Inc. with the FDA for Fortex Pedicle Screw System.
Device ID | K090224 |
510k Number | K090224 |
Device Name: | FORTEX PEDICLE SCREW SYSTEM |
Classification | Orthosis, Spondylolisthesis Spinal Fixation |
Applicant | X-SPINE SYSTEMS, INC. 452 ALEXANDERSVILLE RD. Miamisburg, OH 45342 |
Contact | David Kirschman |
Correspondent | David Kirschman X-SPINE SYSTEMS, INC. 452 ALEXANDERSVILLE RD. Miamisburg, OH 45342 |
Product Code | MNH |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-01-30 |
Decision Date | 2009-07-30 |
Summary: | summary |