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 |