# K955914: Limited Reuse Arthroscopic Blades

- Pathway: 510(k) (Traditional)
- Applicant: Smith & Nephew Dyonics, Inc.
- Decided: Feb 8, 1996 after 55 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 3 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K023777: Arthronet Blackline 2 and 3 Piece Arthroscopic Blades, Models 123, 133, 153, 163, 173 and 183 (2002), 1 descendant of its own
- K060172: Rema Shaver Blades (2006), 0 descendants of its own
- K971676: Limited Reuse Endoscopic Blades (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K955914
Methodology: https://510kreport.com/methodology