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AESCULAP
Aesculap AG · Model FK651R · UDI-DI 04046964072611
KBJ
Prescription
1
510(k) clearances
2
Adverse events
1
Recalls
77
Facilities
Description
Bone Curette, angled, 7 1/2", (190 mm), oval, width: 4 mm, non-sterile, reusable
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2004-01-29 | Medtronic Xomed, Inc. | The box label indicates that the product is a size 2 whereas a size 4 was packed inside. |
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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.