In2Bones
IN2BONES · Model G02 00021 · UDI-DI 03760225714577
GFG
Prescription
3
510(k) clearances
697
Adverse events
17
Recalls
101
Facilities
Description
REAMER 2IN1 DIAM 2.2 LG 11 MM AO STERILE CANNULATED LG65 MM
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
| 2017-03-15 | Smith & Nephew, Inc. | Potential for the cutting blade to detach from the device and/or the distal drill head to fracture during retrograde reaming |
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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.