# K040076: Anspach Advanced Micro Saw Attachments

- Pathway: 510(k) (Traditional)
- Applicant: The Anspach Effort, Inc.
- Decided: Mar 15, 2004 after 61 days
- Product code: HBE (Drills, Burrs, Trephines & Accessories (Simple, Powered))
- Device class: 2
- Regulation: 21 CFR 882.4310
- Recalls of this device: 3 (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. The FDA summary names its predicate without a number.
- (no number) Anspach Micro Saws: named in the summary without a submission number

## Recalls of this device
- Nov 28, 2012 · Class II · Z-1882-2014: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were not manufactured consistently with Quality System requirements.
- Nov 28, 2012 · Class II · Z-1884-2014: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were not manufactured consistently with Quality System requirements.
- Nov 28, 2012 · Class II · Z-1883-2014: The Anspach Effort, Inc. in Palm Beach Gardens, FL is recalling their Anspach Custom Devices. The units were not manufactured consistently with Quality System requirements.

## Indications for use
Anspach micro saw attachments are indicated for use with eMax electrical and Black Max, MicroMax pneumatic drill systems for surgical cutting, shaping and removal of bone, including bones of the spine and cranium.

Source page: https://510kreport.com/device/K040076
Methodology: https://510kreport.com/methodology