T10 Screwdriver, Solid

GUDID 00848665028782

ADVANCED ORTHOPEDIC SOLUTIONS INC

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile Surgical screwdriver, single-use, non-sterile

Primary Device ID	00848665028782
NIH Device Record Key	930f84c2-db99-4212-97a7-1bf6983a593f
Commercial Distribution Status	In Commercial Distribution
Brand Name	T10 Screwdriver, Solid
Version Model Number	5020
Company DUNS	117858154
Company Name	ADVANCED ORTHOPEDIC SOLUTIONS 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	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com
Phone	3105339966
Email	regaffairs@aosortho.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00848665028782 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K163014

FDA Product Code

HSB	Rod, Fixation, Intramedullary And Accessories