FDA UDI In Commercial Distribution 🇺🇸 United States

RESPONSE 5.5/6.0 SYSTEM

DI: 00841132145807 · Model: 00-1600-0025 · ORTHOPEDIATRICS CORP.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RESPONSE 5.5/6.0 SYSTEM
Primary DI
00841132145807
Version / Model
00-1600-0025
Company Name
ORTHOPEDIATRICS CORP.
Labeler DUNS
796416191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-03-28
Public Version
3
Public Version Date
2020-09-10
Public Version Status
Update
Public Device Record Key
7fa564de-56a0-4c0d-8ebb-135f593676fa

Device Description

S-ROD, Ø 6.0MM COCR, 400MM, 50MM STRAIGHT

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
Yes
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
NKB Thoracolumbosacral pedicle screw system
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
37272 Trans-facet-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00841132145807

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K150600 000
K181390 000
K193100 000