The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Zimmer Anatomic Hip System.
| Device ID | K922071 |
| 510k Number | K922071 |
| Device Name: | ZIMMER ANATOMIC HIP SYSTEM |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
| Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Contact | Angie Ide |
| Correspondent | Angie Ide ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
| Product Code | LPH |
| CFR Regulation Number | 888.3358 [🔎] |
| Decision | Substantially Equivalent - Kit (SESK) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-05-04 |
| Decision Date | 1994-02-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024136397 | K922071 | 000 |
| 00889024136199 | K922071 | 000 |
| 00889024136175 | K922071 | 000 |
| 00889024136151 | K922071 | 000 |
| 00889024136137 | K922071 | 000 |
| 00889024136113 | K922071 | 000 |
| 00889024136090 | K922071 | 000 |
| 00889024136076 | K922071 | 000 |
| 00889024136052 | K922071 | 000 |
| 00889024136038 | K922071 | 000 |
| 00889024136021 | K922071 | 000 |
| 00889024136212 | K922071 | 000 |
| 00889024136236 | K922071 | 000 |
| 00889024136250 | K922071 | 000 |
| 00889024136380 | K922071 | 000 |
| 00889024136373 | K922071 | 000 |
| 00889024136366 | K922071 | 000 |
| 00889024136359 | K922071 | 000 |
| 00889024136342 | K922071 | 000 |
| 00889024136335 | K922071 | 000 |
| 00889024136328 | K922071 | 000 |
| 00889024136311 | K922071 | 000 |
| 00889024136298 | K922071 | 000 |
| 00889024136274 | K922071 | 000 |
| 00889024136014 | K922071 | 000 |