Protek, Inc.
Protek, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 1989.
Top product codes for Protek, Inc.
Recent clearances by Protek, Inc.
- K893785 — ARC-2F ACETABULAR CUP
- K893959 — P.S.A. FEMORAL HIP PROSTHESIS
- K892059 — FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
- K883794 — RESUBMITTED CLW ACETABULAR CUP W/SULMESH
- K884952 — VARIOUS FEMORAL HIP PROSTHESES W/SELF LOCK CERAMIC
- K884889 — MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.
- K884789 — NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI
- K890054 — M.E.M. ACETABULAR CUP W/SULMESH FOR CEMENT APPLI.
- K884888 — MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
- K882671 — SAMUELSON SCREWLOC CUP
- K874093 — SLS-88 TOTAL HIP SYSTEM, ACETABULAR CUP
- K870922 — C.L.E. ACETABULAR CUP
- K873429 — FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE
- K872985 — SAMUELSON ACETABULAR CUP
- K870923 — SCHUSTER ACETABULAR CUP FOR CEMENT/CEMENTLESS FIX.
- K870924 — CLX ACETABULAR CUP (WAGNER) FOR CEMENTLESS FIXAT.
- K872502 — M.W.P. WRIST PROSTHESIS
- K871347 — WAGNER REVISIONAL FEMORAL HIP PROSTHESIS
- K861988 — MODIFIED PROTASUL 100 (TI-6A1-7NB) ALLOY
- K862752 — C.S.M. HIP
- K853730 — FREEMAN-SAMUELSON MARK II PRESS-FIT TOTAL KNEE REP
- K853768 — MULLER SELF LOCKING TOTAL HIP
- K853662 — MUELLER CURVED STEM HEMI-PROSTHESIS
- K853267 — DAY STAPLE
- K853268 — FREEMAN UNI-COMPARTMENTAL KNEE
Data sourced from openFDA. This site is unofficial and independent of the FDA.