FDA Device Intelligence
HomeASPEN SURGICAL PRODUCTS, INC. › Symmetry Saunders-Paparella

Symmetry Saunders-Paparella

ASPEN SURGICAL PRODUCTS, INC. · Model 61-3740 · UDI-DI 00887482116173

GAC Prescription
2
510(k) clearances
32
Adverse events
1
Recalls
180
Facilities

Description

Symmetry® Window, Saunders-Paparella

Recalls

DateFirmReason
2011-12-29Stryker Howmedica Osteonics Corp.Stryker Orthopaedics has become aware of the potential for the above noted Accolade Rasp Handle Assembly to fracture upon use.

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 docs
Data 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.