FDA Device Intelligence
Home › Pioneer Surgical Technology, Inc. › CONTACT® IBF PEEK VBR/IBF SYSTEM

CONTACT® IBF PEEK VBR/IBF SYSTEM

Pioneer Surgical Technology, Inc. · Model 34-WINDOW30-12 · UDI-DI 00846468037314

MAXMQPODP Prescription
10
510(k) clearances
9,238
Adverse events (30 deaths)
0
Recalls
424
Facilities

Description

DISTRACTION WINDOW

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.