The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Aleuttian.
Device ID | K103169 |
510k Number | K103169 |
Device Name: | ALEUTTIAN |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | K2M, INC. 751 MILLER DR.,SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M, INC. 751 MILLER DR.,SE Leesburg, VA 20175 |
Product Code | ODP |
Subsequent Product Code | MAX |
Subsequent Product Code | MQP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-10-27 |
Decision Date | 2011-03-07 |
Summary: | summary |