Home › ORTHOPEDIATRICS CORP. › OrthoPediatrics PediFoot Deformity Correction System
OrthoPediatrics PediFoot Deformity Correction System
ORTHOPEDIATRICS CORP. · Model 01-1007-0003 · UDI-DI 00841132145050
LHX
Prescription
4
510(k) clearances
102
Adverse events
1
Recalls
1
Facilities
Description
FOOT PUSHER HANDLE
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-01-18 | Stryker Spine | Stryker Spine received reports of packaging failures during shipping for the Jam Shidi instruments, which may compromise the sterility of the product. |
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.