8.5 x 65mm CANN EXTENSION FASTENER 101-85065

GUDID 00810097802087

8.5 x 65mm CANN EXTENSION FASTENER

SMV SCIENTIFIC LLC

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile

Primary Device ID	00810097802087
NIH Device Record Key	89888aad-f55e-4b6c-9d61-b16bc060e8f9
Commercial Distribution Status	In Commercial Distribution
Brand Name	8.5 x 65mm CANN EXTENSION FASTENER
Version Model Number	101-85065
Catalog Number	101-85065
Company DUNS	089645059
Company Name	SMV SCIENTIFIC LLC
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	false
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	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com
Phone	1-800-969-0639
Email	quality@osteocentric.com

Device Dimensions

Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter
Outer Diameter	8.5 Millimeter
Length	65 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810097802087 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K221332

FDA Product Code

NKB	Thoracolumbosacral Pedicle Screw System