Depth Gauge 321-0005

GUDID 00810074300971

Depth Gauge

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

Primary Device ID	00810074300971
NIH Device Record Key	d81fefdd-d45c-4fec-9d78-d80da1baa151
Commercial Distribution Status	In Commercial Distribution
Brand Name	Depth Gauge
Version Model Number	321-0005
Catalog Number	321-0005
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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810074300971 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K150981

FDA Product Code

HWC	Screw, Fixation, Bone