FDA applicant
Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech
FDA records 2 decisions for Pioneer Surgical Technology, Inc D.B.A Resolve Surgical Tech (Marquette, MI) from 2022 to 2023: 2 510(k) clearances. Most are in product codes HRS (Plate, Fixation, Bone) and KWQ (Appliance, Fixation, Spinal Intervertebral Body). Its devices cite 2 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 D.B.A Resolve Surgical Tech’s devices, and how often a recall has named them.
FDA decisions per year
1in 2023
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2022.
Planning a device like Pioneer Surgical Technology, Inc D.B.A…’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.