The following data is part of a premarket notification filed by Exactech, Inc. with the FDA for Exactech Acapella One Cervical Spacer System.
Device ID | K132582 |
510k Number | K132582 |
Device Name: | EXACTECH ACAPELLA ONE CERVICAL SPACER SYSTEM |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Contact | Patrick Hughes |
Correspondent | Patrick Hughes EXACTECH, INC. 2320 N.W. 66TH CT. Gainesville, FL 32653 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-08-16 |
Decision Date | 2014-02-12 |
Summary: | summary |