FDA Device Intelligence
HomeSTRYKER CORPORATION › NA

NA

STRYKER CORPORATION · Model 0296097102 · UDI-DI 04546540895042

DWH Prescription
4
510(k) clearances
159
Adverse events (1 deaths)
1
Recalls
35
Facilities

Description

Sternum Blade, Offset (31.5 x 0.64 x 6.2mm)

Recalls

DateFirmReason
2011-11-17Terumo Cardiovascular Systems CorporationTerumo Cardiovascular Systems has received one report of minute metal shavings leaking from the Sarns Sternal Saw I System at the point where the saw blade is inserted into the saw

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.