PMA P010014S043
- Device
- OXFORD PARTIAL KNEE SYSTEM
- Applicant
- Biomet Manufacturing Corp
- PMA number
- P010014
- Supplement
- S043
- Product code
- NRA
- Decision date
- 2013-06-25
- Classification
- Prosthesis, Knee, Femorotibial, Unicompartmental, Semi-constrained, Metal/polymer, Mobile Bearing
- Generic name
- Prosthesis, knee, femorotibial, unicompartmental, semi-constrained, metal/polymer, mobile bearing
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT BIOMET, INC., WARSAW, INDIANA, FOR MANUFACTURING OF THE MENISCAL BEARINGS.
Current openFDA PMA Record#
- Device
- OXFORD PARTIAL KNEE SYSTEM
- Applicant
- Biomet Manufacturing Corp
- PMA number
- P010014
- Supplement
- S043
- Product code
- NRA
- Generic name
- Prosthesis, knee, femorotibial, unicompartmental, semi-constrained, metal/polymer, mobile bearing
- Decision date
- 2013-06-25
- Decision code
- APPR
- Date received
- 2013-04-22
- Supplement type
- Normal 180 Day Track No User Fee
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AT BIOMET, INC., WARSAW, INDIANA, FOR MANUFACTURING OF THE MENISCAL BEARINGS.