The following data is part of a premarket notification filed by Depuy Spine, Inc. with the FDA for Pipeline Ii Access System.
| Device ID | K062814 |
| 510k Number | K062814 |
| Device Name: | PIPELINE II ACCESS SYSTEM |
| Classification | Retractor, Self-retaining, For Neurosurgery |
| Applicant | DEPUY SPINE, INC. 325 PARAMOUNT DR. Raynham, MA 02767 |
| Contact | Sharon Starowicz |
| Correspondent | Sharon Starowicz DEPUY SPINE, INC. 325 PARAMOUNT DR. Raynham, MA 02767 |
| Product Code | GZT |
| CFR Regulation Number | 882.4800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-09-20 |
| Decision Date | 2006-12-15 |
| Summary: | summary |