Spine Smith Partners LP

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0932-2013Class IICynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemenAugust 24, 2012