Triage Medical, Inc.
FDA 510(k) medical device clearances.
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.