The following data is part of a premarket notification filed by X-spine Systems, Inc. with the FDA for Butrex Buttress Plating System.
Device ID | K072943 |
510k Number | K072943 |
Device Name: | BUTREX BUTTRESS PLATING SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
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 | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2007-10-17 |
Decision Date | 2008-01-28 |
Summary: | summary |