K040080 is an FDA 510(k) clearance for the AESCULAP ABSORBABLE CRANIOFIX. This device is classified as a Cover, Burr Hole (Class II - Special Controls, product code GXR).
Submitted by Aesculap, Inc. (Center Valley, US). The FDA issued a Cleared decision on March 31, 2004, 76 days after receiving the submission on January 15, 2004.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.5250.
| 510(k) Number | K040080 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 15, 2004 |
| Decision Date | March 31, 2004 |
| Days to Decision | 76 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | GXR — Cover, Burr Hole |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.5250 |