The following data is part of a premarket notification filed by Pioneer Surgical Technology, Inc. Dba Rti Surgical, Inc. with the FDA for Streamline Navigated Instruments.
| Device ID | K200095 |
| 510k Number | K200095 |
| Device Name: | Streamline Navigated Instruments |
| Classification | Orthopedic Stereotaxic Instrument |
| Applicant | Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc. 375 River Park Circle Marquette, MI 49855 |
| Contact | Kurtis Hunsberger |
| Correspondent | Kurtis Hunsberger Pioneer Surgical Technology, Inc. DBA RTI Surgical, Inc. 375 River Park Circle Marquette, MI 49855 |
| Product Code | OLO |
| CFR Regulation Number | 882.4560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-01-16 |
| Decision Date | 2020-06-26 |