STOMA® micro-screw 23061.13

GUDID ESAM23061130

stoma® micro-screw, inner square, Ø 1,2mm, 13mm, 3 pcs are developed and manufactured to be used as non-active bone surgery implants for the treatment of bone fractures in the dental field. They are recommended especially for the fixation of transplanted bone blocks and small grafts during the augmentation process in the oral cavity and maxillomandibular surgical field, e.g. for horizontal, vertical or 3D augmentative grafts. The small-sized diameter of the screw head enables various applications. STOMA® micro-screws are delivered in non-sterile conditions.

Storz am Mark GmbH

Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable Craniofacial bone screw, non-bioabsorbable

Primary Device ID	ESAM23061130
NIH Device Record Key	b04960c9-eae4-4901-a5da-0ee6cf5abf20
Commercial Distribution Status	In Commercial Distribution
Brand Name	STOMA® micro-screw
Version Model Number	23061.13
Catalog Number	23061.13
Company DUNS	318268125
Company Name	Storz am Mark GmbH
Device Count	3
DM Exempt	true
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	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de
Phone	+49746592600
Email	sam@stoma.de

Device Dimensions

Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter
Length	13 Millimeter
Outer Diameter	1.2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	ESAM23061130 [Unit of Use]
HIBCC	ESAM23061131 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K080430

FDA Product Code

DZL	Screw, Fixation, Intraosseous