K953969 is an FDA 510(k) clearance for the PRECLUDE DURA SUBSTITUTE. This device is classified as a Dura Substitute (Class II - Special Controls, product code GXQ).
Submitted by W.L. Gore & Associates, Inc. (Elkton, US). The FDA issued a Cleared decision on November 1, 1995, 71 days after receiving the submission on August 22, 1995.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.5910.
| 510(k) Number | K953969 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 22, 1995 |
| Decision Date | November 01, 1995 |
| Days to Decision | 71 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | GXQ — Dura Substitute |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 882.5910 |