The following data is part of a premarket notification filed by Osteonics Corp. with the FDA for Silkon Stainless Steel Cable System.
| Device ID | K962132 |
| 510k Number | K962132 |
| Device Name: | SILKON STAINLESS STEEL CABLE SYSTEM |
| Classification | Cerclage, Fixation |
| Applicant | OSTEONICS CORP. 2 PEARL COURT Allendale, NJ 07401 -1677 |
| Contact | Charles Ryan |
| Correspondent | Charles Ryan OSTEONICS CORP. 2 PEARL COURT Allendale, NJ 07401 -1677 |
| Product Code | JDQ |
| CFR Regulation Number | 888.3010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-06-03 |
| Decision Date | 1996-08-08 |
| Summary: | summary |