AccessGUDID - DEVICE: PANTA (10381780044505)

GUDID

Device Identifier (DI) Information

Brand Name: PANTA
Version or Model: 500080ND
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 500080ND
Company Name: NEWDEAL

Primary DI Number: 10381780044505
Issuing Agency: GS1
Commercial Distribution End Date: April 19, 2027
Device Count: 1
Labeler D-U-N-S® Number*: 536935331 *Terms of Use

Device Description: The NEWDEAL Ankle Nail is a straight, cannulated intramedullary nail available in diameters of 10mm, 11mm, 12mm and 13mm, and lengths of 150mm, 180mm, 210mm and 240mm. Holes in the nail allow for proximal and distal locking, using locking cortical screws 5mm diameter, 20 to 110mm long. The nail is made from Titanium alloy.

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":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
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?
44854	Arthrodesis intramedullary nail, non-distracting	A rigid rod, not intended for bone distraction, dedicated to arthrodesis/joint fusion through implantation into the intramedullary canal of a long bone [e.g., femur, tibia, humerus (including fixation of the glenoid), fibula, radius, ulna] which extends beyond the joint to an adjacent bone(s), as part of traumatic repair or reconstructive procedures. It may be of fixed or variable length to allow compression (dynamic). It is intended to be fixed to the bone with screws which may be included with the nail. This is a single-use device.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
HSB	ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K091788	000

Device Exempt from Premarket Submission: No CLOSE

Sterilization

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

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Special Storage Condition, Specify: Store in dry place

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 10mm diam. x 183mm length

Device Record Status

Public Device Record Key: 52638ce5-27b6-4e5b-95d1-30a83352f805
Public Version Date: February 06, 2025
Public Version Number: 7
DI Record Publish Date: October 09, 2017