FDA UDI Not in Commercial Distribution 🇺🇸 United States

LCP

DI: 10886982162144 · Model: 238.705S · SYNTHES (U.S.A.) LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
LCP
Primary DI
10886982162144
Version / Model
238.705S
Catalog Number
238705S
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
2023-09-18
Public Version Status
Update
Public Device Record Key
27aa7a70-35fa-4f1b-8a70-5f754ae2ca02
Distribution End Date
2019-09-22

Device Description

3.5MM LCP(TM) MEDIAL DISTAL TIBIA PL W/O TAB 8H/LT-STER

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
HRS PLATE, FIXATION, BONE

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Secondary H679238705S0
Primary 10886982162144

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K013248 000