K870844 is an FDA 510(k) clearance for the SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTOR. This device is classified as a Extractor (Class I - General Controls, product code HWB).
Submitted by Warsaw Orthopedic, Inc. (Warsaw, US). The FDA issued a Cleared decision on March 13, 1987, 10 days after receiving the submission on March 3, 1987.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.4540.
| 510(k) Number | K870844 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | March 03, 1987 |
| Decision Date | March 13, 1987 |
| Days to Decision | 10 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | HWB — Extractor |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 888.4540 |