# K964252: Orthochuck

- Pathway: 510(k) (Traditional)
- Applicant: Buckman Co., Inc.
- Decided: May 27, 1997 after 215 days
- Product code: GEY (Motor, Surgical Instrument, Ac-Powered)
- 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) Jacob’s chuck key: named in the summary without a submission number

## Indications for use
Converts All Standard Keyed Metal Chuck Head Surgical Drives Into Keyless Chuck Drives.

Source page: https://510kreport.com/device/K964252
Methodology: https://510kreport.com/methodology