ARMAR / ARTIS Small Fragment and Calcaneal Plates & MBOSS / FIXION Screws, ARMAR/ ARTIS Humerus and Olecranon Plates & MBOSS/FIXION Screws, ARMAR / ARTIS Tibia and Buttress Plates & MBOSS/FIXION Screws, ARMAR / ARTIS 2.4mm Plates & MBOSS/FIXION Screws, ARMAR/ ARTISClavical Hook Plate & MBOSS/FIXION Screws, ARMAR/ ARTIS Metaphyseal Plate & MBOSS/FIXION Screws, ARMAR / ARTISCalcaneal Plate & MBOSS/FIXION Screws
K171320 is the FDA 510(k) clearance record for ARMAR / ARTIS Small Fragment and Calcaneal Plates & MBOSS / FIXION Screws, ARMAR/ ARTIS Humerus and Olecranon Plates & MBOSS/FIXION Screws, ARMAR / ARTIS Tibia and Buttress Plates & MBOSS/FIXION Screws, ARMAR / ARTIS 2.4mm Plates & MBOSS/FIXION Screws, ARMAR/ ARTISClavical Hook Plate & MBOSS/FIXION Screws, ARMAR/ ARTIS Metaphyseal Plate & MBOSS/FIXION Screws, ARMAR / ARTISCalcaneal Plate & MBOSS/FIXION Screws, a class II device, cleared for Meril Healthcare Pvt. , Ltd. on under FDA product code HRS (Plate, Fixation, Bone). FDA records list 7 510(k) clearances for Meril Healthcare Pvt. , Ltd., from to . As of , FDA records show no recalls naming K171320.
Clearance record
- Decision date
- Received
- (308 days to decision)
- Product code
- HRS Plate, Fixation, Bone
- Regulation
- 21 CFR 888.3030
- Device class
- Class II
- Review panel
- Orthopedic
- Applicant
- Meril Healthcare Pvt. , Ltd. First Floor, H1-H3, Meril Park,, Muktanand Marg, Chala, Vapi, IN
- 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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