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FREER KILLIAN ELEVATOR

SONTEC INSTRUMENTS, INC. · Model 412-535T · UDI-DI 00192896100718

HTE Prescription
0
510(k) clearances
137
Adverse events (1 deaths)
3
Recalls
175
Facilities

Description

FREER KILLIAN ELEVATOR DOUBLE-ENDED TITANIUM

Recalls

DateFirmReason
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.
2013-09-24SpineFrontier, Inc.Handles and heads may not be compatible.

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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.