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Electro-Biology, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
28
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K992333EBI OMEGA 21 SYSTEMOctober 8, 1999
K992367EBI XFIX DYNAFIX SYSTEM HA COATED SCREWSSeptember 23, 1999
K991941EBI XFIX DFS RAIL SYSTEMAugust 19, 1999
K990303EBI OMEGA 21 SYSTEMApril 29, 1999
K991092EBI SPINELINK ANTERIOR CERVICAL SPINAL SYSTEMApril 29, 1999
K990459EBI VUECATH ENDOSCOPIC SYSTENApril 23, 1999
K990999MODIFICATION OF: EBI SPINELINK SYSTEMApril 14, 1999
K984027EBI SPINELINK SYSTEMJanuary 19, 1999
K982484EBI VUECATH ENDOSCOPIC SPINAL SYSTEMOctober 8, 1998
K982908MODIFICATION TO EBI SPINELINK SYSTEMAugust 28, 1998
K981483EBI DFS JOINT FIXATOR, MODEL 02800July 8, 1998
K971970EBI SPINELINK SYSTEMAugust 20, 1997
K971083ARTHROSCOPEJune 23, 1997
K964797EBI SPINELINK SYSTEMMay 2, 1997
K964533EBI SPINELINK SYSTEMApril 9, 1997
K963261EBI THERMAL THERAPY SYSTEMSeptember 27, 1996
K961433EBI X FIX DYNAFIX SYSTEM/EBI DFS DISTAL RADIUS FIXATOR SC BONE SCREWSJune 28, 1996
K955730EBI ANTERIOR CERVICAL SPINE SYSTEMMarch 13, 1996
K953406EBI X FIX DYNAFIX SYSTEM (DFS)October 31, 1995
K953532EBICEOctober 4, 1995