# Protek, Inc.

- Location (FDA's records): Indianapolis, IN
- FDA decisions: 25 (1985–1989): 25 510(k) clearances
- Product codes: JDI (7), KWA (4), KWL (3), MBV (2), LWJ (2), KWM (1), HSX (1), LZO (1), JDR (1), KWY (1), LZY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Biocore9, LLC: 1 (https://510kreport.com/company/biocore9)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Engineering Consulting Services, Inc.: 1 (https://510kreport.com/company/engineering-consulting-services)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)

## Its most-cited devices
- K853730: Freeman-Samuelson Mark II Press-Fit Total Knee Rep (1986), cited by 2
- K884888: Modified New Jersey Acetabular Comp. & Bone Screws (1988), cited by 1
- K871347: Wagner Revisional Femoral Hip Prosthesis (1987), cited by 1

## Recent decisions
- K893785: Arc-2F Acetabular Cup (Aug 9, 1989)
- K893959: P.S.a. Femoral Hip Prosthesis (Jul 25, 1989)
- K892059: Femoral Heads/Modular & Fixed W/ Titan Nitride Sur (Jul 19, 1989)
- K883794: Resubmitted CLW Acetabular Cup W/Sulmesh (May 26, 1989)
- K884952: Various Femoral Hip Prostheses W/Self Lock Ceramic (May 10, 1989)
- K884889: Modified O.E.C. Univ. Self-Aligning Aceta. Comp. (Feb 27, 1989)
- K890054: M.E.M. Acetabular Cup W/Sulmesh for Cement Appli. (Feb 8, 1989)
- K884789: New Jersey Femoral Hip Prosthesis for Cement Appli (Feb 8, 1989)

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