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 |