K032331 is an FDA 510(k) clearance for the DORO RADIOLUCENT HEADREST SYSTEM AND HORSESHOE HEADRESTS,AND NON-RADIOLUCENT J-ARM RETRACTOR SYSTEM (ALUMINUM ALLOY). This device is classified as a Holder, Head, Neurosurgical (skull Clamp) (Class II — Special Controls, product code HBL).
Submitted by Pro-Med Instruments GmbH (Alva, US). The FDA issued a Cleared decision on November 20, 2003, 114 days after receiving the submission on July 29, 2003.
This device falls under the Neurology FDA review panel. Regulated under 21 CFR 882.4460.
| 510(k) Number | K032331 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 29, 2003 |
| Decision Date | November 20, 2003 |
| Days to Decision | 114 days |
| Submission Type | Traditional |
| Review Panel | Neurology (NE) |
| Summary | Summary PDF |
| Product Code | HBL — Holder, Head, Neurosurgical (skull Clamp) |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 882.4460 |