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Guided Growth Plate System
ORTHOFIX SRL · Model 1 · UDI-DI 18054242513360
OBT
Prescription
1
510(k) clearances
10
Adverse events
1
Recalls
21
Facilities
Description
Quad - plate guided growth plate 16 mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-05 | Wishbone Medical, Inc. | The products in this lot are incorrectly packed with a Stainless-Steel implant instead of a Titanium implant as the packaging and part number indicated. |
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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.