FDA Import Refusal AEK-2318343-4/1/1 — ORCHID Orthopedic Solutions, Ltd.

ORCHID Orthopedic Solutions, Ltd. — FEI 3010089671

The FDA refused shipment AEK-2318343-4/1/1 from ORCHID Orthopedic Solutions, Ltd. (United Kingdom) on Jun 19, 2017. The refused product falls under Devices — PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/. Cited charge: 118 This firm has 3 other import refusals on record.

Refusal details

Date
Jun 19, 2017
Country
United Kingdom
Product Category
Devices
Product Code
87MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/
Charges
118

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.