# K982375: Stryker Hip Arthoroscopy Set

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Endoscopy
- Decided: Oct 2, 1998 after 87 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
Longest line of descent: 3 generations back to K833587 (1983). 15 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963524: Ksea Large Joint Arthroscopy Set, Karl Storz Endoscopy (1996) Summary page 1.
- K971253: Various Arthroscopes, Endoscopic Blades, Manual Instruments, Smith & Nephew, Inc. (1997) Summary page 1.
- K926212: Arthrex Instruments ( Hip ), Arthrex, Inc. (1994) Summary page 1.

## Most influential descendants
- K012635: Reprocessed Stryker Arthroscopic Shavers (2001), 0 descendants of its own
- K012605: Reprocessed Athroscopics Burs (2001), 0 descendants of its own

## Indications for use
The Stryker Hip Arthroscopy Set, consisting of reusable instrumentation to access, illuminate and visualize the confines of the hip joint, is indicated for operative and diagnostic arthroscopic procedures of hip joint pathology including evaluation and the removal of loose bodies. Resection of soft, osseous and cartilaginous tissues is possible when used in conjunction with Stryker sterile disposable Rotary Hip Surgical Blades.

Source page: https://510kreport.com/device/K982375
Methodology: https://510kreport.com/methodology