Primary Device ID | B562PKSFP3506TUS0 |
NIH Device Record Key | c66a444d-f5d2-41ee-bd92-3f579c2b6f89 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Procedure Kit, Straight Fibula Plate, 6 hole, 3.5mm Cortical Screws, Ti |
Version Model Number | PK-SFP3506T-US |
Company DUNS | 062355158 |
Company Name | WISHBONE MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
B56251300MDG000G10 - WishBone Plate & Screw System | 2024-01-09 Medium Depth Gauge (65mm) |
B56211705310200S0 - Smart Correction | 2023-07-03 3.0/200/10mm Half Pin, Self-Drilling/Self-Tapping, QC, SS, HA |
B56211705315200S0 - Smart Correction | 2023-07-03 3.0/200/15mm Half Pin, Self-Drilling/Self-Tapping, QC, SS, HA |
B56211705320200S0 - Smart Correction | 2023-07-03 3.0/200/20mm Half Pin, Self-Drilling/Self-Tapping, QC, SS, HA |
B56211705325200S0 - Smart Correction | 2023-07-03 3.0/200/25mm Half Pin, Self-Drilling/Self-Tapping, QC, SS, HA |
B56211705330200S0 - Smart Correction | 2023-07-03 3.0/200/30mm Half Pin, Self-Drilling/Self-Tapping, QC, SS, HA |
B56211705335200S0 - Smart Correction | 2023-07-03 3.0/200/35mm Half Pin, Self-Drilling/Self-Tapping, QC, SS, HA |
B56211705340200S0 - Smart Correction | 2023-07-03 3.0/200/40mm Half Pin, Self-Drilling/Self-Tapping, QC, SS, HA |