FDA Registration Active 🇺🇸 United States

BIOMET MODULAR FEMORAL REVISION SYSTEM

Reg #: 3005061536 · FEI: 3005061536 · Expires 2025
Products
9
Proprietary Names
2
Establishment Types
1
Classifications
9

Registration Details

Registration Name
SYMMETRY MEDICAL MANUFACTURING INC
Registration Number
3005061536
FEI Number
3005061536
Status
Active
Expiry Year
2025
Initial Importer
No
Address
111 N. CLAY
City
CLAYPOOL
State
IN
ZIP
46510
Country
US

Regulatory Submissions

510(k) Number
K090757

Owner / Operator

Firm Name
Tecomet
Operator Number
1828464
Address
170 New Boston Street, --
City
Woburn
State
MA
Postal Code
01801
Country
US

Products

Device Name Product Code
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented LPH
Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component) KWA
Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate MEH
Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) JDL
Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented JDI
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish MAY
Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented KWY
Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer KWZ
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented LZO

Proprietary Names

BIOMET MODULAR FEMORAL REVISION SYSTEM prosthesis, hip, semi-constrained (metal uncemented acetabular component)

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer)