# General and Plastic Surgery Devices; Reclassification of Certain Surgical Staplers
> **Food and Drug Administration** · Final amendment; final order. · Published 2021-10-08 · Effective 2021-10-08 · 86 FR 56195
## Document
- **Document number:** 2021-22041
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 86 FR 56195
- **CFR reference:** 21 CFR 878
- **Publication date:** 2021-10-08
- **Effective date:** 2021-10-08
- **HHS docket:** Docket No. FDA-2019-N-1250
## Abstract

The Food and Drug Administration (FDA or the Agency) is issuing a final order to reclassify surgical staplers for internal use (formerly regulated under the classification for "manual surgical instrument for general use" and assigned the product code GAG) from class I (general controls) into class II (special controls) and subject to premarket review. FDA is identifying the special controls for surgical staplers for internal use that the Agency believes are necessary to provide a reasonable assurance of the safety and effectiveness of the device. FDA is issuing this reclassification on its own initiative based on new information. As part of this reclassification, FDA is also amending the existing classification for "manual surgical instrument for general use" to remove staplers and to create a separate classification regulation for surgical staplers that distinguishes between surgical staplers for internal use and external use.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2021/10/08/2021-22041/general-and-plastic-surgery-devices-reclassification-of-certain-surgical-staplers)
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