FDA Registration Active 🇨🇭 Switzerland

TRYPTIK

Reg #: 3007728266 · FEI: 3007728266 · Expires 2025
Products
1
Proprietary Names
1
Establishment Types
2
Classifications
1

Registration Details

Registration Name
SPINEART SA
Registration Number
3007728266
FEI Number
3007728266
Status
Active
Expiry Year
2025
Initial Importer
No
Address
Chemin du Pre-Fleuri 3
City
Plan-les-Ouates Geneve
Country
CH

Regulatory Submissions

510(k) Number
K122366

Owner / Operator

Firm Name
SPINEART SA
Operator Number
10028947
Address
Chemin du Pre-Fleuri 3
City
Plan-les-Ouates
State
Geneve
Postal Code
1228
Country
CH
Correspondent
Max LOK

Products

Device Name Product Code
Intervertebral Fusion Device With Bone Graft, Cervical ODP

Proprietary Names

TRYPTIK

Establishment Types

Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility