FDA Registration Active 🇺🇸 United States

Patient-Specific Implant (PSI) System

Reg #: 3017048829 · FEI: 3017048829 · Expires 2025
Products
3
Proprietary Names
1
Establishment Types
1
Classifications
3

Registration Details

Registration Name
LINEAR PRECISION, INC.
Registration Number
3017048829
FEI Number
3017048829
Status
Active
Expiry Year
2025
Initial Importer
No
Address
1838 A Habersham Square
City
Florence
State
SC
ZIP
29501
Country
US

Regulatory Submissions

510(k) Number
K241077

Owner / Operator

Firm Name
Linear Precision, Inc.
Operator Number
10075737
Address
1838 A Habersham Square
City
Florence
State
SC
Postal Code
29501
Country
US
Correspondent
Jessica McCracken

Products

Device Name Product Code
Intervertebral Fusion Device With Bone Graft, Thoracic PHM
Intervertebral Fusion Device With Integrated Fixation, Lumbar OVD
Intervertebral Fusion Device With Bone Graft, Lumbar MAX

Proprietary Names

Patient-Specific Implant (PSI) System

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer)