FDA UDI Not in Commercial Distribution 🇺🇸 United States

CapSure® Spine System

DI: 10840642104868 · Model: 11-3541 · Spine Wave, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CapSure® Spine System
Primary DI
10840642104868
Version / Model
11-3541
Catalog Number
11-3541
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2019-12-18
Public Version Status
Update
Public Device Record Key
8ea36a0a-3822-4184-84c6-245627994b50
Distribution End Date
2019-12-17

Device Description

PS2 Screw 5.5mm x 40mm

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
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

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

Identifiers

Type ID
Primary 10840642104868

Customer Contacts

Phone
203-944-9494

Premarket Submissions

Submission Number Supplement Number
K081228 000

Device Sizes

Type Value Unit Text
Outer Diameter 5.5 Millimeter
Length 40 Millimeter