PMA P010014S028
- Device
- OXFORD PARTIAL KNEE SYSTEM
- Applicant
- Biomet Manufacturing Corp
- PMA number
- P010014
- Supplement
- S028
- Product code
- NRA
- Decision date
- 2011-01-07
- 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 CHANGES TO THE PACKAGE INSERT, INCLUDING THE ADDITION OF MR CONDITIONAL LABELING AND THE ASSOCIATED MR CONDITIONS OF USE.
Current openFDA PMA Record#
- Device
- OXFORD PARTIAL KNEE SYSTEM
- Applicant
- Biomet Manufacturing Corp
- PMA number
- P010014
- Supplement
- S028
- Product code
- NRA
- Generic name
- Prosthesis, knee, femorotibial, unicompartmental, semi-constrained, metal/polymer, mobile bearing
- Decision date
- 2011-01-07
- Decision code
- APPR
- Date received
- 2010-11-09
- Supplement type
- Real-Time Process
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Approval order statement
- APPROVAL FOR CHANGES TO THE PACKAGE INSERT, INCLUDING THE ADDITION OF MR CONDITIONAL LABELING AND THE ASSOCIATED MR CONDITIONS OF USE.