FDA UDI In Commercial Distribution 🇺🇸 United States

SYNERGY

DI: 03596010459657 · Model: 71309010 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
SYNERGY
Primary DI
03596010459657
Version / Model
71309010
Catalog Number
71309010
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
6
Public Version Date
2025-07-09
Public Version Status
Update
Public Device Record Key
c1d8c5da-6f96-4384-9deb-89a44a1adb9c

Device Description

SYNERGY POROUS PLUS HA STANDARD OFFSET SIZE 10

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
MR Conditional
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
No

Product Codes

Code Name
MEH Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate

GMDN Terms

Code Name
38155 Press-fit femoral stem prosthesis

Identifiers

Type ID
Primary 03596010459657

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K002996 000
K211176 000