K802271 is an FDA 510(k) clearance for the THE IMMOBILIZER FOR OPEN & ARTHROSCOPIC. This device is classified as a Table And Attachments, Operating-room (Class I - General Controls, product code BWN).
Submitted by The Anspach Effort, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 23, 1980, 36 days after receiving the submission on September 17, 1980.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4950.
| 510(k) Number | K802271 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 17, 1980 |
| Decision Date | October 23, 1980 |
| Days to Decision | 36 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | — |
| Product Code | BWN — Table And Attachments, Operating-room |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4950 |