FDA product code MRY: Appliances And Accessories, Fixation, Bone, Absorbable Single/Multiple Component
MRY is the FDA product code for appliances and accessories, fixation, bone, absorbable single/multiple component. It is a Class II device, regulated under 21 CFR 888.3040 and reviewed by the Orthopedic panel. Devices under MRY reach the market by 510(k); FDA lists no cleared 510(k)s for it.
Classification
| Field | Value |
|---|---|
| Device name | Appliances And Accessories, Fixation, Bone, Absorbable Single/Multiple Component |
| Device class | Class II |
| Regulation | 21 CFR 888.3040 |
| Review panel | OR — Orthopedic |
| Medical specialty | Orthopedic |
| Premarket route | 510(k) |
| Implant | Yes |
Recalls for MRY devices
openFDA lists no recalls for product code MRY.
Frequently asked questions
What is FDA product code MRY?
MRY is the FDA product code for appliances and accessories, fixation, bone, absorbable single/multiple component. It is a Class II device, regulated under 21 CFR 888.3040 and reviewed by the Orthopedic panel.
What device class is MRY?
Class II, regulation 21 CFR 888.3040. Typical premarket route: 510(k).
Next steps
- Run an FDA pathway report with predicate devices for product code MRY
- Run a recall and safety report across every MRY manufacturer
- Watch product code MRY for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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