Submission Details
| 510(k) Number | K942969 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 20, 1994 |
| Decision Date | July 20, 1994 |
| Days to Decision | 30 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
K942969 is an FDA 510(k) clearance for the AUTO SUTURE SPINAL NERVE HOOK, a Instrument, Surgical, Non-powered (Class I — General Controls, product code HAO), submitted by United States Surgical, A Division of Tyco Healthc (Norwalk, US). The FDA issued a Cleared decision on July 20, 1994, 30 days after receiving the submission on June 20, 1994. This device falls under the Neurology review panel. Regulated under 21 CFR 882.4535.
| 510(k) Number | K942969 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | June 20, 1994 |
| Decision Date | July 20, 1994 |
| Days to Decision | 30 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | HAO — Instrument, Surgical, Non-powered |
| Device Class | Class I — General Controls |
| CFR Regulation | 21 CFR 882.4535 |