FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 10886982239723 · Model: 5213-52 · SYNTHES (U.S.A.) LP
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982239723
Version / Model
5213-52
Catalog Number
521352
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
6
Public Version Date
2019-12-23
Public Version Status
Update
Public Device Record Key
40fcdfc2-7bfc-4b09-b8ff-0dadf18bbe76
Distribution End Date
2019-12-04

Device Description

GLENOID 52MM-STERILE

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWT PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED
HSD PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED
MBF PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED

GMDN Terms

Code Name
36259 Shoulder glenoid fossa prosthesis, prefabricated

Identifiers

Type ID
Secondary H6795213520
Primary 10886982239723

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072578 000