Spine-Tech, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K980288SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEMJuly 29, 1998
K970040SPINE-TECH BONE HARVESTERFebruary 28, 1997
K951268SPINE-TECH MODIFIED LAPAROSCOPIC SPINAL FUSION INSTRUMENT SYSTEMJuly 31, 1995
K940913SPINE-TECH LAPAROSCOPIC INSTRUMENTATION SYSTEMOctober 4, 1994