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Synthes GmbH · Model 292.656 · UDI-DI 10886982180797

LRNHTY Prescription
8
510(k) clearances
1,208
Adverse events (2 deaths)
1
Recalls
39
Facilities

Description

2.0MM NON-THREADED GUIDE WIRE- SPADE POINT ON ONE END 230MM

Recalls

DateFirmReason
2019-09-10Exactech, Inc.Potential for the wire to fracture at the threads and remain in the glenoid.

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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.