AccessGUDID - DEVICE: SURFIX (10381780044451)

GUDID

Device Identifier (DI) Information

Brand Name: SURFIX
Version or Model: PTFGND
Commercial Distribution Status: In Commercial Distribution
Catalog Number: PTFGND
Company Name: NEWDEAL

Primary DI Number: 10381780044451
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2027
Device Count: 1
Labeler D-U-N-S® Number*: 536935331 *Terms of Use

Device Description: The SURFIX Knee Osteotomy System consists of different stainless steel plates for the proximal tibia and the distal femur with a locking system between the threaded sockets of the plates and the lock screws. Their fixation is provided by titanium alloy screws and lock screws available in two versions : cancellous bone screws diameter 6.5 mm and cortical bone screws diameter 4.5 mm. The system fixation creates a single implant/screw unit fixed into the bone thanks to the lock screw.

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:	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?
46647	Orthopaedic fixation plate, non-bioabsorbable	A non-bioabsorbable, non-customized, firm, implantable sheet intended to stabilize a fractured orthopaedic bone (excluding craniofacial and spinal) to treat a traumatic/pathological fracture, to fuse a joint (arthrodesis) and/or as part of an osteotomy. Typically attached to a bone of a limb, rib, sternum, or pelvis, it is designed to be fixed in place with screws, and may be used in connection with another fixation plate; it does not incorporate a sleeve or blade. Disposable instruments intended to facilitate implantation, or fixation implants (i.e., bone screws), may be packaged with the plate.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
HRS	PLATE, FIXATION, BONE

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K041601	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: Must be stored in a dry, cool place away from dust and UV radiation

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: c903a551-a707-4da9-990b-6f3a832762f9
Public Version Date: November 20, 2025
Public Version Number: 8
DI Record Publish Date: October 09, 2017