FDA UDI In Commercial Distribution 🇺🇸 United States

INTEGRATE-C

DI: G2308HT0910S100 · Model: Trial - Small 15 x 12 x 9/10 mm, 10 deg · Happe Spine, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INTEGRATE-C
Primary DI
G2308HT0910S100
Version / Model
Trial - Small 15 x 12 x 9/10 mm, 10 deg
Catalog Number
T090S1
Company Name
Happe Spine, LLC
Labeler DUNS
118446952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-24
Public Version
2
Public Version Date
2023-12-18
Public Version Status
Update
Public Device Record Key
705a8c8a-5103-4887-891e-8dc64ef29d58

Device Description

Trial - small footprint 10deg, 9/10 height

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
LYQ Accessories, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
64192 Internal spinal fixation procedure kit, reusable

Identifiers

Type ID
Primary G2308HT0910S100

Customer Contacts

Phone
616-984-0204

Premarket Submissions

Submission Number Supplement Number
K222004 000