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 |