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Periosteal Elevator

I.T.S. GmbH · Model KM 46-211 · UDI-DI 09120034306174

HTE
0
510(k) clearances
138
Adverse events (1 deaths)
3
Recalls
175
Facilities

Description

Periosteal Elevator, 6mm Straight Edge

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.