# K962800: Stryker Universal Drill Attachments & Accessories

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Instruments
- Decided: Sep 11, 1996 after 55 days
- Product code: HWE (Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment)
- Device class: 1
- Regulation: 21 CFR 878.4820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Powered instrument attachments marketed by Midas Rex: named in the summary without a submission number
- (no number) Powered instrument attachments marketed by Codman: named in the summary without a submission number
- (no number) Pre-1976 medical device amendment cutting accessories distributed by Stryker: named in the summary without a submission number
- (no number) Cutting accessories distributed by Midas Rex: named in the summary without a submission number
- (no number) Cutting accessories distributed by Zimmer/Hall: named in the summary without a submission number

## Indications for use
The Stryker Universal Drill Attachments and Accessories are intended for use in the cutting, drilling, reaming, decorticating, and smoothing of bone and other bone related tissue in a variety of surgical procedures including: ENT, orthopedic, maxillofacial, neuro, and plastics.

Source page: https://510kreport.com/device/K962800
Methodology: https://510kreport.com/methodology