Spine Smith Partners LP

FDA Regulatory Profile

Spine Smith Partners LP appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0932-2013, Class II) was initiated on August 24, 2012.

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