Drill Sleeve 120002

GUDID 00816950028038

Drill Sleeve

SMV SCIENTIFIC LLC

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Primary Device ID	00816950028038
NIH Device Record Key	3edfe308-c4b6-47d6-8b2d-ba21f2b0fb22
Commercial Distribution Status	In Commercial Distribution
Brand Name	Drill Sleeve
Version Model Number	120002
Catalog Number	120002
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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816950028038 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K152000

FDA Product Code

HRS	Plate, Fixation, Bone