The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc with the FDA for C-plus.
Device ID | K133623 |
510k Number | K133623 |
Device Name: | C-PLUS |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Contact | Sarah Mcintyre |
Correspondent | Sarah Mcintyre PIONEER SURGICAL TECHNOLOGY, INC 375 RIVER PARK CIRCLE Marquette, MI 49855 |
Product Code | ODP |
Subsequent Product Code | MAX |
Subsequent Product Code | MQP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-11-26 |
Decision Date | 2014-02-10 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
C-PLUS 79084378 3927973 Dead/Cancelled |
COTESI-COMPANHIA DE TÃXTEIS SINTÃTICOS,S.A. 2010-05-05 |
C-PLUS 75315716 not registered Dead/Abandoned |
ORGA KARTENSYSTEME GMBH 1997-06-27 |
C-PLUS 73593370 not registered Dead/Abandoned |
VENTA, INC. 1986-04-14 |
C-PLUS 73265585 1203290 Dead/Cancelled |
Stanley Home Products, Inc. 1980-06-09 |