The following data is part of a premarket notification filed by Pioneer Surgical Technology with the FDA for Pacp System.
| Device ID | K053053 |
| 510k Number | K053053 |
| Device Name: | PACP SYSTEM |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| 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 | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-10-31 |
| Decision Date | 2005-11-16 |
| Summary: | summary |