FDA Registration Active 🇺🇸 United States

HAnano InterFuse® Modular Interbody

Reg #: 3010020754 · FEI: 3010020754 · Expires 2025
Products
1
Proprietary Names
1
Establishment Types
2
Classifications
1

Registration Details

Registration Name
NEXT ORTHOSURGICAL
Registration Number
3010020754
FEI Number
3010020754
Status
Active
Expiry Year
2025
Initial Importer
No
Address
3270 Corporate Vw Ste A
City
Vista
State
CA
ZIP
92081
Country
US

Regulatory Submissions

510(k) Number
K242509

Owner / Operator

Firm Name
Next Orthosurgical
Operator Number
10042957
Address
3270 Corporate View, Suite A
City
Vista
State
CA
Postal Code
92081
Country
US
Correspondent
Misty Calkins

Products

Device Name Product Code
Intervertebral Fusion Device With Bone Graft, Lumbar MAX

Proprietary Names

HAnano InterFuse® Modular Interbody

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device