Symmetry Cloward 57-5583
by Aspen Surgical Products, Inc.
Symmetry Cloward 57-5583 is a Class II device made by Aspen Surgical Products, Inc., cleared under FDA 510(k) K071771 on 2 Aug 2007 and listed in FDA GUDID since 21 Sep 2016 (UDI-DI 00887482098639), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00887482098639 | Date21 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK071771 | Date2 Aug 2007 | StatusActive |
Official records
- AccessGUDID record 00887482098639
- FDA 510(k) database K071771
Across registries
- FDA 510(k) K071771 decided 2 Aug 2007 Active
- FDA GUDID UDI-DI 00887482098639 listed 21 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K071771
- Listed FDA GUDID 00887482098639
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Symmetry Cloward
- Generic name
- Self-retaining surgical retractor, reusable
- Model / Ref / Catalog
- 57-5583
- Primary DI / UDI-DI
- 00887482098639
- 510(k) Number
- FDA product code
- GZT
- GMDN term
- Self-retaining surgical retractor, reusable
- Device class
- Class II
- Regulation number
- 882.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 4.3333 Inch