Triage Medical, Inc.
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K062391 | DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02; COMPRESSION TOOL, MODEL 6113-00 | MRW | 2006-09-14 | View |
| 510(k) | K052043 | 3.8MM CS FACET COMPRESSION DEVICE | MRW | 2005-10-17 | View |
| 510(k) | K051949 | 4.5 MM LS FACET COMPRESSION DEVICE WITH POLYMER WASHER, MODEL LSPW-45-3040 | MRW | 2005-08-05 | View |
| 510(k) | K043351 | 4.5MM BONE-LOK FACET SCREW, MODELS TFCD-45-3040S OR N; SFCD-45-3040S OR N | MRW | 2005-02-18 | View |
| 510(k) | K042244 | BONE-LOK MVP CORTICAL-CANCELLOUS COMPRESSION DEVICE | HWC | 2004-09-16 | View |
| 510(k) | K040250 | BONE-LOK HP WASHER | HTN | 2004-03-23 | View |
| 510(k) | K014304 | BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR, MODEL BMCD-35-3050S | HWC | 2002-03-27 | View |
| 510(k) | K014243 | BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR WITH TITANIUM FIXTURE , MODEL BMCD-35-3040, MBCD-35-4050 | HWC | 2002-03-26 | View |
| 510(k) | K012818 | HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX | HWC | 2001-11-20 | View |
| 510(k) | K012817 | HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED | HWC | 2001-11-20 | View |
| 510(k) | K012280 | TITANIUM COMPRESSION ANCHOR SYSTEM MODEL VERSION 2 | HWC | 2001-08-17 | View |
No matching devices.
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