FDA Registration Active 🇺🇸 United States

Bone Graft, Lumbar Intervertebral Fusion Device

Reg #: 3010120183 · FEI: 3010120183 · Expires 2025
Products
1
Proprietary Names
1
Establishment Types
1
Classifications
1

Registration Details

Registration Name
Judson A Smith Company
Registration Number
3010120183
FEI Number
3010120183
Status
Active
Expiry Year
2025
Initial Importer
No
Address
857 863 Sweinhart and Cleaver Roads
City
Boyertown
State
PA
ZIP
19512
Country
US

Regulatory Submissions

510(k) Number
K120203

Owner / Operator

Firm Name
Judson A Smith Company
Operator Number
10043835
Address
857-863 Sweinhart and Cleaver Roads
City
Boyertown
State
PA
Postal Code
19512
Country
US
Correspondent
Caryn Mitchell

Products

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

Proprietary Names

Bone Graft, Lumbar Intervertebral Fusion Device

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer)