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ANAX™ 5.5 SPINAL SYSTEM
CG MedTech Co.,Ltd. · Model SFM0914 · UDI-DI 08800015960113
FXM
Prescription
1
510(k) clearances
15
Adverse events
5
Recalls
16
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-02-19 | Smith And Nephew, Inc. Endoscopy Division | Endocouplers assembled with screws that cannot be effectively sterilized |
| 2004-02-19 | Smith And Nephew, Inc. Endoscopy Division | Endocouplers assembled with screws that cannot be effectively sterilized |
| 2004-02-19 | Smith And Nephew, Inc. Endoscopy Division | Endocouplers assembled with screws that cannot be effectively sterilized |
| 2004-02-19 | Smith And Nephew, Inc. Endoscopy Division | Endocouplers assembled with screws that cannot be effectively sterilized |
| 2004-02-19 | Smith And Nephew, Inc. Endoscopy Division | Endocouplers assembled with screws that cannot be effectively sterilized |
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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.