APS Osteotomy Fixation System (0945-1302-xx /4.5mm Cortex Screw); APS Osteotomy Fixation System (0850-4302-xx / 5.0mm Locking Screw); APS Osteotomy Fixation System (0701-xx10(1)-05 / Proximal Medial Tibial Osteotomy Locking Plate); APS Osteotomy Fixation System (0701-xx60(1)-0x / Proximal Medial Tibial Osteotomy Locking Plate, Small); APS Osteotomy Fixation System (0702-xx00(1)-03 / Proximal Lateral Tibial Osteotomy Locking Plate); APS Osteotomy Fixation System (0501-xx00(1)-04 / Dista
K252897 is the FDA 510(k) clearance record for APS Osteotomy Fixation System (0945-1302-xx /4.5mm Cortex Screw); APS Osteotomy Fixation System (0850-4302-xx / 5.0mm Locking Screw); APS Osteotomy Fixation System (0701-xx10(1)-05 / Proximal Medial Tibial Osteotomy Locking Plate); APS Osteotomy Fixation System (0701-xx60(1)-0x / Proximal Medial Tibial Osteotomy Locking Plate, Small); APS Osteotomy Fixation System (0702-xx00(1)-03 / Proximal Lateral Tibial Osteotomy Locking Plate); APS Osteotomy Fixation System (0501-xx00(1)-04 / Dista, a class II device, cleared for A Plus Biotechnology Co., Ltd. on under FDA product code HRS (Plate, Fixation, Bone). FDA records list 3 510(k) clearances for A Plus Biotechnology Co., Ltd., from to . As of , FDA records show no recalls naming K252897.
Clearance record
- Decision date
- Received
- (91 days to decision)
- Product code
- HRS Plate, Fixation, Bone
- Regulation
- 21 CFR 888.3030
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- A Plus Biotechnology Co., Ltd. 3f., # 23, Qiaohe Rd., Zhonghe Dist., New Taipei City, TW
- 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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