FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10887587055763 · Model: 487.962 · SYNTHES (U.S.A.) LP
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10887587055763
Version / Model
487.962
Catalog Number
487962
Company Name
SYNTHES (U.S.A.) LP
Labeler DUNS
832637081
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
5
Public Version Date
2022-10-10
Public Version Status
Update
Public Device Record Key
be0c42ee-8ed5-4838-94d8-0e8693d18d33
Distribution End Date
2017-04-15

Device Description

TI SINGLE VECTOR DISTRACTOR BODY WITH RIGHT FOOT/20MM

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MQN EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR
JEY PLATE, BONE

GMDN Terms

Code Name
47635 Implantable craniofacial bone distractor

Identifiers

Type ID
Primary 10887587055763
Secondary H9804879620

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K022005 000
K981075 000