FDA Registration Active 🇺🇸 United States

aprevo® lateral lumbar interbody fusion device

Reg #: 3017936978 · FEI: 3017936978 · Expires 2025
Products
1
Proprietary Names
3
Establishment Types
2
Classifications
1

Registration Details

Registration Name
CARLSMED, INC.
Registration Number
3017936978
FEI Number
3017936978
Status
Active
Expiry Year
2025
Initial Importer
No
Address
1800 Aston Avenue, Suite 100
City
Carlsbad
State
CA
ZIP
92008
Country
US

Regulatory Submissions

510(k) Number
K222082

Owner / Operator

Firm Name
Carlsmed, Inc.
Operator Number
10080208
Address
1800 Aston Avenue, Suite 100
City
Carlsbad
State
CA
Postal Code
92008
Country
US
Correspondent
Mike Cordonnier

Products

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

Proprietary Names

aprevo® lateral lumbar interbody fusion device aprevo® transforaminal lumbar interbody fusion device aprevo® anterior lumbar interbody fusion device

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device