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devemed GmbH · Model PPS 1000 F · UDI-DI 04061644021079

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

Description

PPS | Periosteal elevator "Salama"# 1 for lateral tunnel procedures | 2 mm F-LINE | SL | double ended

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.