FDA UDI In Commercial Distribution 🇺🇸 United States

VA-LCP

DI: 10886982054487 · Model: 02.211.251 · Synthes GmbH
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VA-LCP
Primary DI
10886982054487
Version / Model
02.211.251
Catalog Number
02211251
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
8
Public Version Date
2024-02-27
Public Version Status
Update
Public Device Record Key
fc1296ac-c394-4804-ae5c-6aa122dffc32

Device Description

2.4/2.7MM VA-LCP CLOVERLEAF FUSION PLATE/STANDARD

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
HRS PLATE, FIXATION, BONE
HWC Screw, fixation, bone

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Secondary H679022112510
Primary 10886982054487

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K100776 000