# K953868: Grasping Forceps, Biopsy Forceps, Scissors, Punch

- Pathway: 510(k) (Traditional)
- Applicant: Richard Wolf Medical Instruments Corp.
- Decided: Sep 29, 1995 after 43 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: 1 (0 Class I)
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Jul 24, 2017 · Class II · Z-2897-2018: Punch may have a burr in one section of the joint and when the punch is open, there is an increase potential for injury.

Source page: https://510kreport.com/device/K953868
Methodology: https://510kreport.com/methodology