The following data is part of a premarket notification filed by Depuy Orthopaedics, Inc. with the FDA for Depuy Aml Hip Prosthesis.
| Device ID | K061833 |
| 510k Number | K061833 |
| Device Name: | DEPUY AML HIP PROSTHESIS |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
| Contact | Anne Schuler |
| Correspondent | Anne Schuler DEPUY ORTHOPAEDICS, INC. 700 ORTHOPAEDIC DRIVE Warsaw, IN 46581 -0988 |
| Product Code | LPH |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-06-29 |
| Decision Date | 2006-07-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10603295058359 | K061833 | 000 |
| 10603295058335 | K061833 | 000 |
| 10603295058236 | K061833 | 000 |
| 10603295058212 | K061833 | 000 |