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 |