AccessGUDID - DEVICE: Solar™ Interbody Fusion System (00842048180531)

GUDID

Device Identifier (DI) Information

Brand Name: Solar™ Interbody Fusion System
Version or Model: 1205-5528
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 1205-5528
Company Name: DEGEN MEDICAL, INC.

Primary DI Number: 00842048180531
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 078812602 *Terms of Use

Device Description: Fixed Anterior Lumbar Screw, Self Tapping 5.5x28mm

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?
46651	Spinal bone screw, non-bioabsorbable	A small, threaded, implantable rod with a screw head and drive intended for internal spinal fixation by being screwed into the spine to hold a correction/stabilization device (e.g., rod, plate, tether) to bone; it is made of a material that is not chemically degraded or absorbed via natural body processes (e.g., surgical steel, titanium alloy, carbon fibre). It is available in various types (e.g., pedicle or transfacet, with a slotted, cross, star, or polygonal drive), and is typically used to provide immobilization and stabilization of spinal segments in the treatment of spinal instabilities or deformities. A screw head adaptor intended to stabilize a rod may be included with the screw.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
PHM	Intervertebral fusion device with bone graft, thoracic
MAX	Intervertebral fusion device with bone graft, lumbar
OVD	Intervertebral fusion device with integrated fixation, lumbar

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K231199	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
Device Size Text, specify: Diameter (5.5 Millimeter);Length (28 Millimeter)

Device Record Status

Public Device Record Key: fa6f4c9b-da71-49cf-a289-1dce3a22f2f4
Public Version Date: September 11, 2024
Public Version Number: 4
DI Record Publish Date: July 15, 2023