FDA 510(k) Applications Submitted by Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K192718 | 09/27/2019 | Fortilink Interbody Fusion Device (IBF) with TETRAfuse 3D Technology | Pioneer Surgical Technology, Inc., DBA RTI Surgical, Inc. |
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