FDA UDI In Commercial Distribution 🇺🇸 United States

Apelo® / Apelo® MIS

DI: M68169063306500 · Model: 6906-33-0650 · ATLAS SPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Apelo® / Apelo® MIS
Primary DI
M68169063306500
Version / Model
6906-33-0650
Catalog Number
6906-33-0650
Company Name
ATLAS SPINE, INC.
Labeler DUNS
140801007
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
5
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
ab1629ce-a3ca-403c-8238-87c8cb438503

Device Description

6.5mm Reduction Mono Screw Kit

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
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
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

Code Name
56642 Orthopaedic bone screw, non-bioabsorbable, non-sterile

Identifiers

Type ID
Primary M68169063306500

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K072426 000