The following data is part of a premarket notification filed by X-spine Systems, Inc. with the FDA for Spider Cervical Plating (scp) System.
| Device ID | K052292 |
| 510k Number | K052292 |
| Device Name: | SPIDER CERVICAL PLATING (SCP) SYSTEM |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | X-SPINE SYSTEMS, INC. 7026 CORPORATE WAY # 212 Centerville, OH 45459 -4288 |
| Contact | David Kirschman |
| Correspondent | David Kirschman X-SPINE SYSTEMS, INC. 7026 CORPORATE WAY # 212 Centerville, OH 45459 -4288 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-08-23 |
| Decision Date | 2005-10-21 |
| Summary: | summary |