TriMed ASET Foot Plating System (1ST MTP 9-hole Long Plate), TriMed ASET Foot Plating System (1st Met Osteotomy Plate), TriMed ASET Foot Plating System (H-Plate), TriMed ASET Foot Plating System (Talonavicular Plate), TriMed ASET Foot Plating System (Calcaneal Slide Osteotomy Plate), TriMed ASET Foot Plating System (Evans Osteotomy Plate), TriMed ASET Foot Plating System (Medial Column Fusion Plate), TriMed ASET Foot Plating System (Straight Plate), TriMed ASET Foot Plating System (T-
K233863 is the FDA 510(k) clearance record for TriMed ASET Foot Plating System (1ST MTP 9-hole Long Plate), TriMed ASET Foot Plating System (1st Met Osteotomy Plate), TriMed ASET Foot Plating System (H-Plate), TriMed ASET Foot Plating System (Talonavicular Plate), TriMed ASET Foot Plating System (Calcaneal Slide Osteotomy Plate), TriMed ASET Foot Plating System (Evans Osteotomy Plate), TriMed ASET Foot Plating System (Medial Column Fusion Plate), TriMed ASET Foot Plating System (Straight Plate), TriMed ASET Foot Plating System (T-, a class II device, cleared for TriMed, Inc. on under FDA product code HRS (Plate, Fixation, Bone). FDA records list 38 510(k) clearances for TriMed, Inc., from to . As of , FDA records show no recalls naming K233863.
Clearance record
- Decision date
- Received
- (133 days to decision)
- Product code
- HRS Plate, Fixation, Bone
- Regulation
- 21 CFR 888.3030
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- TriMed, Inc. 27533 Ave. Hopkins, Santa Clarita CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code HRS
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 5 |
| December 2025 | 5 |
| January 2026 | 4 |
| February 2026 | 5 |
| March 2026 | 13 |
| April 2026 | 6 |
| May 2026 | 2 |
| June 2026 | 5 |
| July 2026 | 5 |
| August 2026 | 3 |
| September 2026 | 4 |
| October 2026 | 0 |
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