Triage Medical, Inc. is one of 22816 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Triage Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02, 3.8MM CS FACET COMPRESSION DEVICE, 4.5 MM LS FACET COMPRESSION DEVICE WITH POLYMER WASHER, MODEL LSPW-45-3040
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
Cleared
Sep 14, 2006
DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND...
Orthopedic
29d
Cleared
Oct 17, 2005
3.8MM CS FACET COMPRESSION DEVICE
Orthopedic
81d
Cleared
Aug 05, 2005
4.5 MM LS FACET COMPRESSION DEVICE WITH POLYMER WASHER, MODEL LSPW-45-3040
Orthopedic
21d
Cleared
Feb 18, 2005
4.5MM BONE-LOK FACET SCREW, MODELS TFCD-45-3040S OR N
Orthopedic
74d
Cleared
Sep 16, 2004
BONE-LOK MVP CORTICAL-CANCELLOUS COMPRESSION DEVICE
Orthopedic
28d
Cleared
Mar 23, 2004
BONE-LOK HP WASHER
Orthopedic
50d
Cleared
Mar 27, 2002
BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR, MODEL BMCD-35-3050S
Orthopedic
86d
Cleared
Mar 26, 2002
BONE-LOK BIOABSORBABLE COMPRESSION ANCHOR WITH TITANIUM FIXTURE , MODEL...
Orthopedic
90d
Cleared
Nov 20, 2001
HELICAL COMPRESSION ANCHOR SYSTEM, NON-CANNULATED
Orthopedic
90d
Cleared
Nov 20, 2001
HELICAL COMPRESSION ANCHOR SYSTEM, CANNULATED SINGLE HELIX
Orthopedic
90d
Cleared
Aug 17, 2001
TITANIUM COMPRESSION ANCHOR SYSTEM MODEL VERSION 2
Orthopedic
29d