The following data is part of a premarket notification filed by Kinamed, Inc. with the FDA for Kinematch Patello-femoral Resurfacing Impalant.
| Device ID | K013982 |
| 510k Number | K013982 |
| Device Name: | KINEMATCH PATELLO-FEMORAL RESURFACING IMPALANT |
| Classification | Prosthesis, Knee, Patello/femoral, Semi-constrained, Cemented, Metal/polymer |
| Applicant | KINAMED, INC. 820 FLYNN RD. Camarillo, CA 93012 |
| Contact | Vineet Sarin |
| Correspondent | Vineet Sarin KINAMED, INC. 820 FLYNN RD. Camarillo, CA 93012 |
| Product Code | KRR |
| CFR Regulation Number | 888.3540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-12-03 |
| Decision Date | 2002-05-21 |