Jace Systems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K933059ARTROMOT-E, ELBOW / ARTROMOT-S, SHOULDER CMP MOD.June 22, 1994
K931016JACE MODEL H440 HAND CPM DEVICEJune 22, 1994
K931781JACE TRI-STIM DEVICEOctober 8, 1993
K922185JACE KNEE EXTENSION SYSTEM -- MODIFICATIONJune 11, 1992
K921351JACE MODEL PM-410 HAND CPM DEVICEMay 4, 1992
K920380JACE MODEL W550 WRIST CPM DEVICEFebruary 11, 1992