Home › Corentec Co., Ltd › LOSPA Knee System, EXULT Knee System
LOSPA Knee System, EXULT Knee System
Corentec Co., Ltd · Model KA.CPC.0002C · UDI-DI 08800017205267
LHX
Prescription
4
510(k) clearances
102
Adverse events
1
Recalls
1
Facilities
Description
Patella Clamp Resection Guide Head 2
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.