AccessGUDID - DEVICE: OSSDSIGN Cranioplug (07350086550252)

GUDID

Device Identifier (DI) Information

Brand Name: OSSDSIGN Cranioplug
Version or Model: 11 mm, 6 fixation-points
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Ossdsign AB

Primary DI Number: 07350086550252
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2022
Device Count: 1
Labeler D-U-N-S® Number*: 350354370 *Terms of Use

Device Description: OSSDSIGN Cranioplug is an osteoconductive calcium phosphate ceramic plug reinforced with a titanium mesh plate which together provide the mechanical performance, safety and efficacy properties. The fully cured calcium phosphate ceramic fills the void in the burr hole. The osteoconductive ceramic component of Cranioplug resorbs and is replaced with bone during the healing process. Cranioplug is sized to match standard 11mm and 14mm burr hole perforators. (510(k) no. K181539)

Device Characteristics

What MRI safety information does the labeling contain?	MR Conditional
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?
46642	Craniofacial fixation plate, non-bioabsorbable, non-customized	A small, implantable, non-customized sheet of firm material designed to be attached with screws to craniofacial bone (including the maxilla and/or mandible) to bridge and stabilize a fracture gap or craniotomy flap, cover a burr hole and/or position/stabilize a prosthesis. It is made of non-bioabsorbable materials (e.g., surgical steel, titanium alloy) and is available in a variety of designs (e.g., Y-plate, curved plate, mesh-panel, burr hole cover). Instruments intended to facilitate implantation (e.g., driver), or plate fixation implants (i.e., bone screws), may be packaged with the plate.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
GXR	Cover, Burr Hole

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: Yes 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
Storage Environment Temperature: between 40 and 93 Degrees Fahrenheit
Storage Environment Temperature: between 4 and 34 Degrees Celsius

Clinically Relevant Size

[?]

Size Type Text
Device Size Text, specify: 6 fixation-points
Outer Diameter: 11 Millimeter

Device Record Status

Public Device Record Key: 60af97f6-bdb6-4914-a3cd-f247cc6d919c
Public Version Date: June 09, 2025
Public Version Number: 7
DI Record Publish Date: June 05, 2019

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
17350086550259	10	07350086550252	2022-12-31	Not in Commercial Distribution	Box
27350086550256	1	07350086550252	2022-12-31	Not in Commercial Distribution	Envelope