Instratek, Inc.
Instratek, Inc. holds FDA 510(k) medical device clearances, first cleared 1992, most recent 2014.
Top product codes for Instratek, Inc.
Recent clearances by Instratek, Inc.
- K133523 — STAPIX SUPERELASTIC IMPLANT BONE STAPLES
- K131620 — JONES-FX FRACTURE SYSTEM
- K120493 — MINI CANNULATED HEADED AND HEADLESS SCREW SET
- K111032 — CMC CABLE FIX
- K091763 — MICHELANGELO BUNION SYSTEM - MABS, MODEL: MA6000
- K082384 — HAV-LOK BUNION CORRECTION SYSTEM
- K080280 — SUB-TALAR LOK, MODEL 7-11 MM
- K940230 — ENDOSCOPIC MORTONS NEUROMA INSTRUMENTS
- K925083 — ENDOTRAK SYSTEM
- K922391 — ENDOSCOPIC CARPAL TUNNEL INSTRUMENTS
Data sourced from openFDA. This site is unofficial and independent of the FDA.