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Phantom Fiber™ Suture - Needled
TORNIER, INC. · Model SMSB0112N · UDI-DI 00846832011674
NWJ
Prescription
9
510(k) clearances
92
Adverse events
1
Recalls
3
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-02-08 | Tornier, Inc | Data has shown that degradation of a raw material used in Phantom Fiber may occur more quickly than expected if improperly stored. This may impact the shelf-life of the product wh |
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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.