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 |