The following data is part of a premarket notification filed by Pioneer Surgical Technology with the FDA for Posterior Cable Screw.
| Device ID | K022908 |
| 510k Number | K022908 |
| Device Name: | POSTERIOR CABLE SCREW |
| Classification | Orthosis, Spinal Pedicle Fixation |
| Applicant | PIONEER SURGICAL TECHNOLOGY 375 RIVER PARK CIRCLE Marquette, MI 49855 -0627 |
| Contact | Jonathan Gilbert |
| Correspondent | Jonathan Gilbert PIONEER SURGICAL TECHNOLOGY 375 RIVER PARK CIRCLE Marquette, MI 49855 -0627 |
| Product Code | MNI |
| CFR Regulation Number | 888.3070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-09-03 |
| Decision Date | 2004-01-22 |
| Summary: | summary |