The following data is part of a premarket notification filed by Depuy, Inc. with the FDA for Protrusion Cages.
| Device ID | K962007 |
| 510k Number | K962007 |
| Device Name: | PROTRUSION CAGES |
| Classification | Mesh, Surgical, Acetabular, Hip, Prosthesis |
| Applicant | DEPUY, INC. 2747 ARMSTRONG LN. Dayton, OH 45414 |
| Contact | Cheryl Hastings |
| Correspondent | Cheryl Hastings DEPUY, INC. 2747 ARMSTRONG LN. Dayton, OH 45414 |
| Product Code | JDJ |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-05-22 |
| Decision Date | 1996-08-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10603295000662 | K962007 | 000 |
| 10603295000471 | K962007 | 000 |
| 10603295000464 | K962007 | 000 |
| 10603295000457 | K962007 | 000 |
| 10603295000440 | K962007 | 000 |
| 10603295000433 | K962007 | 000 |
| 10603295000426 | K962007 | 000 |
| 10603295000419 | K962007 | 000 |
| 10603295000402 | K962007 | 000 |
| 10603295000396 | K962007 | 000 |
| 10603295000389 | K962007 | 000 |
| 10603295000372 | K962007 | 000 |
| 10603295000365 | K962007 | 000 |
| 10603295000358 | K962007 | 000 |
| 10603295000341 | K962007 | 000 |
| 10603295000334 | K962007 | 000 |
| 10603295000488 | K962007 | 000 |
| 10603295000495 | K962007 | 000 |
| 10603295000501 | K962007 | 000 |
| 10603295000655 | K962007 | 000 |
| 10603295000648 | K962007 | 000 |
| 10603295000631 | K962007 | 000 |
| 10603295000624 | K962007 | 000 |
| 10603295000617 | K962007 | 000 |
| 10603295000600 | K962007 | 000 |
| 10603295000594 | K962007 | 000 |
| 10603295000587 | K962007 | 000 |
| 10603295000570 | K962007 | 000 |
| 10603295000563 | K962007 | 000 |
| 10603295000556 | K962007 | 000 |
| 10603295000549 | K962007 | 000 |
| 10603295000532 | K962007 | 000 |
| 10603295000525 | K962007 | 000 |
| 10603295000518 | K962007 | 000 |
| 10603295000327 | K962007 | 000 |