The following data is part of a premarket notification filed by Kirschner Medical Corp. with the FDA for Kirschner Modular Hip System.
| Device ID | K871401 |
| 510k Number | K871401 |
| Device Name: | KIRSCHNER MODULAR HIP SYSTEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented |
| 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 | JDI |
| CFR Regulation Number | 888.3350 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-04-08 |
| Decision Date | 1987-05-18 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00880304714069 | K871401 | 000 |
| 00880304569485 | K871401 | 000 |
| 00880304569492 | K871401 | 000 |
| 00880304569508 | K871401 | 000 |
| 00880304569522 | K871401 | 000 |
| 00880304569539 | K871401 | 000 |
| 00880304569546 | K871401 | 000 |
| 00880304569560 | K871401 | 000 |
| 00880304569577 | K871401 | 000 |
| 00880304569584 | K871401 | 000 |
| 00880304569478 | K871401 | 000 |