510(k) Report

FDA applicant

Pioneer Surgical Technology, Inc. (Rti Surgical, I

Marquette, MI2 decisions2014–20140 recalls

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, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

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

2014: 2
2014high 2 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Pioneer Surgical Technology, Inc. (Rti Surgical, I by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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.

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Other applicant names beginning “Pioneer”

FDA records each applicant name separately; these may or may not be the same firm.