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Interbody Innovations, Llp

FDA Regulatory Profile

Interbody Innovations, Llp appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 5, 2008.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K081614ZEUS SMALL CERVICAL CAGE AND LARGE, EXTRA LARGE, CURVED AND STRAIGHT LUMBAR CAGESSeptember 5, 2008
K073105PEEK SPINAL SPHERESJanuary 3, 2008
K062992SPINAL SPHERESJuly 27, 2007
K051371INTERBODY INNOVATIONS CEMENT RESTRICTORDecember 6, 2005

FDA data resources