FDA applicant
Pioneer Surgical Technology, Inc. (Rti Surgical, I
FDA records 2 decisions for Pioneer Surgical Technology, Inc. (Rti Surgical, I (Marquette, MI) in 2014: 2 510(k) clearances. Most are in product codes MQV (Filler, Bone Void, Calcium Compound) and KWP (Appliance, Fixation, Spinal Interlaminal). Its devices cite 10 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Pioneer Surgical Technology, Inc. (Rti Surgical, I’s devices, and how often a recall has named them.
FDA decisions per year
2in 2014
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2014.
Planning a device like Pioneer Surgical Technology, Inc. (Rti…’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Pioneer”
FDA records each applicant name separately; these may or may not be the same firm.