FSEClass I

Table, Operating-room, Manual

General, Plastic Surgery · 21 CFR 878.4950

MDR events28All time

Recalls1All time

Registered firms51Currently listed

510(k) clearances13All time

Recent MDR events

28 adverse event reports on file

Event type breakdown

Malfunction17

Injury5

Other4

Unspecified2

Most-reported manufacturers

Steris Corp.5 Steris Corporation3 Steris Corporation - Montgomery3 American Sterilizer Company2 Steris Corp2 Unspecified1 Amsco1 Amsco -steris-1

Recalls

1 recall events for this product code

Stryker Medical Div. of Stryker Corporation
TerminatedJun 17, 2006
Stryker Trio Mobile Surgery Platform; Model 1033.
An incorrect pin may have been used during assembly and therefore the device may give way during use.
Z-1155-06 · View FDA record ↗

Registered firms

51 firms currently registered for this product code

510(k) clearances

13 clearances for this product code