K023562 is an FDA 510(k) clearance for the MODIFICATION TO CLASSIC GREAT TOE IMPLANT. This device is classified as a Prosthesis, Toe, Constrained, Polymer (Class II - Special Controls, product code KWH).
Submitted by Nexa Orthopedics, Inc. (Vista, US). The FDA issued a Cleared decision on November 13, 2002, 21 days after receiving the submission on October 23, 2002.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3720.
| 510(k) Number | K023562 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | October 23, 2002 |
| Decision Date | November 13, 2002 |
| Days to Decision | 21 days |
| Submission Type | Special |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | KWH — Prosthesis, Toe, Constrained, Polymer |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3720 |