# Neoligaments, Ltd.

- Location (FDA's records): Leeds, GB
- FDA decisions: 7 (1990–1995): 7 510(k) clearances
- Product codes: JDR (4), HWE (2), HTW (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K941772: Cradle Fixation Device (Aug 7, 1995)
- K952543: Graftologer PGH & Acl Reconstruction Instrument Set (Jun 22, 1995)
- K935753: The Graftologer (Apr 25, 1994)
- K930339: Reamer Bit (Aug 6, 1993)
- K913461: Fastlok (Staple & Buckle) Fixation System (Oct 15, 1991)
- K911445: Fastlok (Staple and Buckle) Fixation System (Jun 28, 1991)
- K904340: Fastlok (Staple and Buckle) Fixation System (Oct 19, 1990)

Source page: https://510kreport.com/company/neoligaments