FDA Import Refusal 799-5646029-3/1/1 — Spineway
The FDA refused shipment 799-5646029-3/1/1 from Spineway (France) on Sep 3, 2014. The refused product falls under Devices — INTERVERTEBRAL BONE GRAFT FUSION DEVICE, CERVICAL. Cited charge: 3280
Refusal details
- Date
- Sep 3, 2014
- Country
- France
- Product Category
- Devices
- Product Code
- 87ODP INTERVERTEBRAL BONE GRAFT FUSION DEVICE, CERVICAL
- Charges
- 3280