FDA UDI Not in Commercial Distribution 🇺🇸 United States

CranioSculpt

DI: 00813845020962 · Model: C-CMF25CC · SKELETAL KINETICS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CranioSculpt
Primary DI
00813845020962
Version / Model
C-CMF25CC
Catalog Number
C-CMF25CC
Company Name
SKELETAL KINETICS LLC
Labeler DUNS
140071411
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-30
Public Version
6
Public Version Date
2021-03-22
Public Version Status
Update
Public Device Record Key
0c89ed20-1f64-47b5-8417-58f2e4522d65
Distribution End Date
2021-01-01

Device Description

CranioSculpt CMF Bone Void Filler

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXP METHYL METHACRYLATE FOR CRANIOPLASTY

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 00813845020962

Customer Contacts

Device Sizes

Type Value Unit Text
Total Volume 25 Milliliter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius