# Orthopaedic Innovations, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 8 (1995–2002): 8 510(k) clearances
- Product codes: JDI (3), HRS (1), KTT (1), KWL (1), LZN (1), LPH (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Fixano SA: 1 (https://510kreport.com/company/fixano)

## Its most-cited devices
- K983881: Cobra External Fixator (1998), cited by 1
- K960014: Practifix External Fixation System (1996), cited by 1
- K962646: Prime Modular Endo Head (1996), cited by 1

## Recent decisions
- K020145: Orthopaedic Innovations Renewal Acetabular Cup System (Apr 15, 2002)
- K983881: Cobra External Fixator (Dec 4, 1998)
- K962646: Prime Modular Endo Head (Sep 23, 1996)
- K960014: Practifix External Fixation System (Mar 18, 1996)
- K955620: Prime Cemented Calcar Femoral Stems (Feb 20, 1996)
- K955751: Prime Femoral Cement Plug (Jan 26, 1996)
- K953033: Prime Cemented Small Femoral Stem (Sep 13, 1995)
- K940328: Prime Cemented Hip System (Apr 7, 1995)

Source page: https://510kreport.com/company/orthopaedic-innovations