FDA UDI In Commercial Distribution 🇺🇸 United States

OASYS

DI: 04546540372000 · Model: 48554406 · Stryker Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
OASYS
Primary DI
04546540372000
Version / Model
48554406
Catalog Number
48554406
Company Name
Stryker Corporation
Labeler DUNS
149183167
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
4
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
0ba7f7b8-3a7d-4196-ad27-abd64b0a427d

Device Description

BONE SCREW

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
Yes
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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
MRW SYSTEM, FACET SCREW SPINAL DEVICE
NKG Orthosis, cervical pedicle screw spinal fixation

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 04546540372000

Device Sizes

Type Value Unit Text
Length 6.0 Millimeter
Device Size Text, specify Diameter: 4.0 Millimeter