Sutter Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K943354SUTTER HAMMERTOE JOINT PROSTHESISJune 12, 1995
K945221SUTTER MODEL 6000 HAND CPM DEVICEFebruary 27, 1995
K931588SUTTER PROXIMAL INTERPHALANGEAL JOINTMarch 10, 1994
K924654FIRST METATARSOPHALANGEAL JOINT MOTION SPLINTFebruary 22, 1993
K914860SUTTER MODEL 10000 LEG CPM DEVICEJanuary 8, 1992
K902707MODEL 9000 AT ANKLE CPM DEVICEJuly 25, 1990
K890607SUTTER HOSPITAL CPMFebruary 27, 1989