The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. (dba Rti Surgical, Inc.) with the FDA for Streamline Oct Occipito-cervico-thoracic System.
| Device ID | K172139 |
| 510k Number | K172139 |
| Device Name: | Streamline OCT Occipito-Cervico-Thoracic System |
| Classification | Posterior Cervical Screw System |
| Applicant | Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) 375 River Park Circle Marquette, MI 49855 |
| Contact | Sarah Pleaugh |
| Correspondent | Sarah Pleaugh Pioneer Surgical Technology, Inc. (DBA RTI Surgical, Inc.) 375 River Park Circle Marquette, MI 49855 |
| Product Code | NKG |
| CFR Regulation Number | 888.3075 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-07-17 |
| Decision Date | 2017-08-18 |
| Summary: | summary |