The following data is part of a premarket notification filed by Zimmer Trabecular Metal Technology with the FDA for Trabecular Metal Fusion Device Model 06-101-xxxxx, 06-102-xxxxx And 08-100-xxxxx.
Device ID | K103033 |
510k Number | K103033 |
Device Name: | TRABECULAR METAL FUSION DEVICE MODEL 06-101-XXXXX, 06-102-XXXXX AND 08-100-XXXXX |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | ZIMMER TRABECULAR METAL TECHNOLOGY 10 POMEROY RD. Parsippany, NJ 07054 |
Contact | Kathleen M Rutherford |
Correspondent | Kathleen M Rutherford ZIMMER TRABECULAR METAL TECHNOLOGY 10 POMEROY RD. Parsippany, NJ 07054 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-10-13 |
Decision Date | 2011-01-10 |
Summary: | summary |