AccessGUDID - DEVICE: 6.0 x 120mm Screw Fastener ST (00816950029295)

GUDID

Device Identifier (DI) Information

Brand Name: 6.0 x 120mm Screw Fastener ST
Version or Model: 360-1120
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 360-1120
Company Name: Osteocentric Technologies, Inc.

Primary DI Number: 00816950029295
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 089645059 *Terms of Use

Device Description: 6.0 x 120mm Screw Fastener ST

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
66947	Orthopaedic bone screw (non-sliding)	A small, threaded, non-bioabsorbable, implantable rod intended for internal orthopaedic fixation by being screwed into a limb bone, rib, the sternum and/or pelvis to hold a plate, nail, rod or prosthesis to the bone, or to provide direct interfragmentary stabilization of a fractured bone; it is not intended to be introduced through the sleeve of a femoral neck fixation plate/sleeve, not used in dentistry/orthodontics, craniofacial or spinal bones, and not dedicated to intramedullary fixation/arthrodesis. It is typically of cortical or cancellous design and has a drive (e.g., slot, cross, star, polygonal) at its proximal end for introduction with a screwdriver.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
JDO	Device, Fixation, Proximal Femoral, Implant

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K210247	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 6.0 Millimeter
Length: 120 Millimeter

Device Record Status

Public Device Record Key: 4d363590-562a-432f-ac01-09e2f3d7f28b
Public Version Date: February 06, 2025
Public Version Number: 5
DI Record Publish Date: May 06, 2021