The following data is part of a premarket notification filed by Biomet Orthopedics, Inc. with the FDA for Ha Pmi Femoral Hip Stem.
| Device ID | K030048 |
| 510k Number | K030048 |
| Device Name: | HA PMI FEMORAL HIP STEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | BIOMET ORTHOPEDICS, INC. 56 EAST BELL DR. P.O. BOX 587 Warsaw, IN 46581 -0587 |
| Contact | Patricia Beres |
| Correspondent | Patricia Beres BIOMET ORTHOPEDICS, INC. 56 EAST BELL DR. P.O. BOX 587 Warsaw, IN 46581 -0587 |
| Product Code | LPH |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-01-06 |
| Decision Date | 2003-02-05 |
| Summary: | summary |