The following data is part of a premarket notification filed by X-spine Systems, Inc with the FDA for Certex Spinal Implant System.
Device ID | K122163 |
510k Number | K122163 |
Device Name: | CERTEX SPINAL IMPLANT SYSTEM |
Classification | Orthosis, Spinal Pedicle 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 | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-07-20 |
Decision Date | 2012-10-31 |
Summary: | summary |