Triage Medical, Inc.
Triage Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2006.
Top product codes for Triage Medical, Inc.
Recent clearances by Triage Medical, Inc.
- K062391 — DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02; COMPRESSION TOOL, MODEL 6113-00
- K052043 — 3.8MM CS FACET COMPRESSION DEVICE
- K051949 — 4.5 MM LS FACET COMPRESSION DEVICE WITH POLYMER WASHER, MODEL LSPW-45-3040
- K043351 — 4.5MM BONE-LOK FACET SCREW, MODELS TFCD-45-3040S OR N; SFCD-45-3040S OR N
- K042244 — BONE-LOK MVP CORTICAL-CANCELLOUS COMPRESSION DEVICE
- K040250 — BONE-LOK HP WASHER
- K014304 — BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR, MODEL BMCD-35-3050S
- K014243 — BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR WITH TITANIUM FIXTURE , MODEL BMCD-35-3040, MBCD-35-4050
- K012817 — HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED
- K012818 — HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX
- K012280 — TITANIUM COMPRESSION ANCHOR SYSTEM MODEL VERSION 2
Data sourced from openFDA. This site is unofficial and independent of the FDA.