Home › ORTHOFIX SRL › Contours Proximal Humeral Plate (Php) & Lsp Titanium Humeral Plate
Contours Proximal Humeral Plate (Php) & Lsp Titanium Humeral Plate
ORTHOFIX SRL · Model 1 · UDI-DI 18032937169337
KTW
Prescription
1
510(k) clearances
910
Adverse events
57
Recalls
51
Facilities
Description
TITANIUM THREAD WIRE L. 120/20 MM THREAD D 2.2 MM (PACK OF 2)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
| 2010-10-27 | Synthes USA (HQ), Inc. | Potential for out of specification star grind teeth. |
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 docsData 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.
