The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Aml Hip Prosthesis.
| Device ID | K012364 |
| 510k Number | K012364 |
| Device Name: | AML HIP PROSTHESIS |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DR. Warsaw, IN 46581 -0988 |
| Contact | Marcia J Arentz |
| Correspondent | Marcia J Arentz DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DR. Warsaw, IN 46581 -0988 |
| Product Code | LPH |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-07-26 |
| Decision Date | 2001-10-19 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10603295058342 | K012364 | 000 |
| 10603295058397 | K012364 | 000 |
| 10603295058380 | K012364 | 000 |
| 10603295058373 | K012364 | 000 |
| 10603295058366 | K012364 | 000 |
| 10603295058304 | K012364 | 000 |
| 10603295058298 | K012364 | 000 |
| 10603295058281 | K012364 | 000 |
| 10603295058274 | K012364 | 000 |
| 10603295058267 | K012364 | 000 |
| 10603295058250 | K012364 | 000 |
| 10603295058403 | K012364 | 000 |
| 10603295058410 | K012364 | 000 |
| 10603295058427 | K012364 | 000 |
| 10603295058328 | K012364 | 000 |
| 10603295058229 | K012364 | 000 |
| 10603295058205 | K012364 | 000 |
| 10603295058502 | K012364 | 000 |
| 10603295058496 | K012364 | 000 |
| 10603295058489 | K012364 | 000 |
| 10603295058472 | K012364 | 000 |
| 10603295058465 | K012364 | 000 |
| 10603295058458 | K012364 | 000 |
| 10603295058441 | K012364 | 000 |
| 10603295058243 | K012364 | 000 |