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InterBRIDGE
LDR Spine Usa, Inc. · Model IB0065T · UDI-DI 03662663004671
PEK
Prescription
10
510(k) clearances
61
Adverse events
1
Recalls
77
Facilities
Description
H6.5mm Insert
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-12-29 | XTANT Medical | The proximal opening of the inserts exhibit an out of specification condition which would prevent the crossbar plates from appropriately engaging with the insert. |
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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.