The following data is part of a premarket notification filed by Osteonics Corp. with the FDA for Osteonics 7000 Series Total Knee Bone Augmentation.
| Device ID | K920524 |
| 510k Number | K920524 |
| Device Name: | OSTEONICS 7000 SERIES TOTAL KNEE BONE AUGMENTATION |
| Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
| Applicant | OSTEONICS CORP. 59 ROUTE 17 Allendale, NJ 07401 -1677 |
| Contact | Robert A Koch |
| Correspondent | Robert A Koch OSTEONICS CORP. 59 ROUTE 17 Allendale, NJ 07401 -1677 |
| Product Code | JWH |
| CFR Regulation Number | 888.3560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-02-05 |
| Decision Date | 1992-05-15 |