The following data is part of a premarket notification filed by Kirschner Medical Corp. with the FDA for Kirschner Bone Fixation Fastener System.
| Device ID | K854445 |
| 510k Number | K854445 |
| Device Name: | KIRSCHNER BONE FIXATION FASTENER SYSTEM |
| Classification | Staple, Fixation, Bone |
| Applicant | KIRSCHNER MEDICAL CORP. 9690 DEERECO ROADD Timonium, MD 21093 |
| Contact | Sam Son |
| Correspondent | Sam Son KIRSCHNER MEDICAL CORP. 9690 DEERECO ROADD Timonium, MD 21093 |
| Product Code | JDR |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1985-11-05 |
| Decision Date | 1985-11-19 |