The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Rush Medullary Pins.
| Device ID | K150626 |
| 510k Number | K150626 |
| Device Name: | Rush Medullary Pins |
| Classification | Pin, Fixation, Smooth |
| Applicant | Zimmer, Inc. P.O. Box 708 Warsaw, IN 46581 |
| Contact | Patrick Mccullagh |
| Correspondent | Stephen H Mckelvey Zimmer, Inc. P.O. Box 708 Warsaw, IN 46581 |
| Product Code | HTY |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-03-11 |
| Decision Date | 2015-05-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024024229 | K150626 | 000 |
| 00889024023697 | K150626 | 000 |
| 00889024023680 | K150626 | 000 |
| 00889024023673 | K150626 | 000 |
| 00889024023666 | K150626 | 000 |
| 00889024023567 | K150626 | 000 |
| 00889024023550 | K150626 | 000 |
| 00889024023543 | K150626 | 000 |
| 00889024023536 | K150626 | 000 |
| 00889024023529 | K150626 | 000 |
| 00889024023512 | K150626 | 000 |
| 00889024023505 | K150626 | 000 |
| 00889024023703 | K150626 | 000 |
| 00889024023710 | K150626 | 000 |
| 00889024023727 | K150626 | 000 |
| 00889024024212 | K150626 | 000 |
| 00889024024069 | K150626 | 000 |
| 00889024024052 | K150626 | 000 |
| 00889024024045 | K150626 | 000 |
| 00889024023482 | K150626 | 000 |
| 00889024024236 | K150626 | 000 |
| 00889024023901 | K150626 | 000 |
| 00889024023895 | K150626 | 000 |
| 00889024023888 | K150626 | 000 |
| 00889024023741 | K150626 | 000 |
| 00889024023734 | K150626 | 000 |
| 00889024023499 | K150626 | 000 |