FDA UDI In Commercial Distribution 🇺🇸 United States

SACRONAIL

DI: 04047844039663 · Model: Locking screw · SIGNUS Medizintechnik GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SACRONAIL
Primary DI
04047844039663
Version / Model
Locking screw
Catalog Number
PBV030050
Company Name
SIGNUS Medizintechnik GmbH
Labeler DUNS
344203948
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-17
Public Version
2
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
a70f3bd8-f1aa-4c55-931a-85bbd57342b4

Device Description

DescriptionThe SACRONAIL system provides a sustained, stable restoration of dorsal pelvic fractures and sacral fractures through its intraosseous location and its direct, bi-iliac symmetric anchorage. The implant consists of a nail of various lengths from135mm to 194mm with a constant diameter of 8mm and 2 locking screws in different lengths. This variation ensures adaptation to the respective anatomy of the patient. The intersections of the screw axes to the implant axis have a distance of 15mm to the respective end face of the nail. This ensures a solid support on the lateral cortex of the Ilia. The angle of the screw axes to the implant axis corresponds to the anatomical conditions and is 70°. The locking screw ensures a stable connection of the components. The tips of the locking screws are rounded to facilitate insertion into the nail while the dorsal ends of locking screws are a hexagon. The caps serve to close the instrument connection of the nail. The implants are made from the Titanium alloy (Ti6Al4V) according to ASTM F 136 / ISO 5832-3, with a Type II anodization according to AMS 2488. There are Instruments which are specific to the implantation of the SACRONAIL device. These include, but are not limited to, the Guide Frame, the Guide Bracket, the Fixation Bracket, various Instrument Guides, various dilators and drills, screwdrivers as well as the specific tools for revision of the device.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HWC Screw, Fixation, Bone
JDS Nail, Fixation, Bone

GMDN Terms

Code Name
63170 Posterior pelvic rod

Identifiers

Type ID
Primary 04047844039663

Customer Contacts

Phone
+49602391660

Premarket Submissions

Submission Number Supplement Number
K212755 000

Device Sizes

Type Value Unit Text
Device Size Text, specify ventral 30mm/dorsal 50mm

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 35 Degrees Celsius