FDA UDI In Commercial Distribution 🇺🇸 United States

Hinged Laminoplasty

DI: 00190837103606 · Model: 174-810PP · Life Spine, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hinged Laminoplasty
Primary DI
00190837103606
Version / Model
174-810PP
Catalog Number
174-810PP
Company Name
Life Spine, Inc.
Labeler DUNS
183641617
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-04
Public Version
1
Public Version Date
2019-11-12
Public Version Status
New
Public Device Record Key
ef0b1afd-2117-4339-b3b5-e4fe9f58dbb0

Device Description

Neutral 10mm Parallel Plate, Parallel Hinge

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
NQW ORTHOSIS, SPINE, PLATE, LAMINOPLASTY, METAL

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00190837103606

Premarket Submissions

Submission Number Supplement Number
K191927 000