The following data is part of a premarket notification filed by Howmedica Osteonics Corp. with the FDA for Avon Patellar Component.
| Device ID | K020841 |
| 510k Number | K020841 |
| Device Name: | AVON PATELLAR COMPONENT |
| Classification | Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer |
| Applicant | HOWMEDICA OSTEONICS CORP. 59 ROUTE 17 SOUTH Allendale, NJ 07401 -1677 |
| Contact | Margaret F Crowe |
| Correspondent | Margaret F Crowe HOWMEDICA OSTEONICS CORP. 59 ROUTE 17 SOUTH Allendale, NJ 07401 -1677 |
| Product Code | KRR |
| CFR Regulation Number | 888.3540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-15 |
| Decision Date | 2002-04-11 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07613327049404 | K020841 | 000 |
| 07613327049350 | K020841 | 000 |
| 07613327049343 | K020841 | 000 |
| 07613327049336 | K020841 | 000 |
| 07613327049329 | K020841 | 000 |
| 07613327049312 | K020841 | 000 |