Home › BOSTON SCIENTIFIC CORPORATION › AdVance™ XP
AdVance™ XP
BOSTON SCIENTIFIC CORPORATION · Model 720163-01 · UDI-DI 00878953005560
OTM
Prescription
10
510(k) clearances
1,525
Adverse events (6 deaths)
1
Recalls
12
Facilities
Description
Male Sling System
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-10-15 | American Medical Systems, Inc. | During routine periodic packaging testing, AMS identified that in simulated extreme shipping and handling situations the sterile barrier packaging of the Needle Passer components s |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.