The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. with the FDA for Pioneer Cannulated Screw System.
| Device ID | K102903 |
| 510k Number | K102903 |
| Device Name: | PIONEER CANNULATED SCREW SYSTEM |
| Classification | Screw, Fixation, Bone |
| Applicant | PIONEER SURGICAL TECHNOLOGY, INC. 375 RIVER PARK CIRCLE Marquette, MI 49855 |
| Contact | Emily M Downs |
| Correspondent | Emily M Downs PIONEER SURGICAL TECHNOLOGY, INC. 375 RIVER PARK CIRCLE Marquette, MI 49855 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-09-30 |
| Decision Date | 2010-10-20 |
| Summary: | summary |