Stryker Orthobiologics, Inc.

FDA Regulatory Profile

Stryker Orthobiologics, Inc. 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-0431-2013, Class II) was initiated on July 26, 2012.

Summary

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

Recent Recalls

NumberClassProductDate
Z-0431-2013Class IIStyker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, sJuly 26, 2012