Medical Device Manufacturer · US , Irvine , CA

Triage Medical, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2001
11
Total
11
Cleared
0
Denied

Triage Medical, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Irvine, US.

Historical record: 11 cleared submissions from 2001 to 2006.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Triage Medical, Inc.
11 devices
1-11 of 11
Cleared Sep 14, 2006
DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND...
K062391 · MRW
Orthopedic · 29d
Cleared Oct 17, 2005
3.8MM CS FACET COMPRESSION DEVICE
K052043 · MRW
Orthopedic · 81d
Cleared Aug 05, 2005
4.5 MM LS FACET COMPRESSION DEVICE WITH POLYMER WASHER, MODEL LSPW-45-3040
K051949 · MRW
Orthopedic · 21d
Cleared Feb 18, 2005
4.5MM BONE-LOK FACET SCREW, MODELS TFCD-45-3040S OR N
K043351 · MRW
Orthopedic · 74d
Cleared Sep 16, 2004
BONE-LOK MVP CORTICAL-CANCELLOUS COMPRESSION DEVICE
K042244 · HWC
Orthopedic · 28d
Cleared Mar 23, 2004
BONE-LOK HP WASHER
K040250 · HTN
Orthopedic · 50d
Cleared Mar 27, 2002
BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR, MODEL BMCD-35-3050S
K014304 · HWC
Orthopedic · 86d
Cleared Mar 26, 2002
BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR WITH TITANIUM FIXTURE , MODEL...
K014243 · HWC
Orthopedic · 90d
Cleared Nov 20, 2001
HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED
K012817 · HWC
Orthopedic · 90d
Cleared Nov 20, 2001
HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX
K012818 · HWC
Orthopedic · 90d
Cleared Aug 17, 2001
TITANIUM COMPRESSION ANCHOR SYSTEM MODEL VERSION 2
K012280 · HWC
Orthopedic · 29d
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