Medical Device Manufacturer · US , Palm Desert , CA

Alphatec Mfg., Inc. - FDA 510(k) Cleared Devices

20 submissions · 18 cleared · Since 1990
20
Total
18
Cleared
0
Denied

Alphatec Mfg., Inc. has 18 FDA 510(k) cleared orthopedic devices. Based in Palm Desert, US.

Historical record: 18 cleared submissions from 1990 to 2004.

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 - Alphatec Mfg., Inc.
20 devices
1-12 of 20
Cleared Mar 26, 2004
ICON POLYAXIAL PEDICLE SCREW SYSTEM
K033090 · KWP
Orthopedic · 179d
Cleared Dec 11, 2002
ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM
K023299 · MNI
Orthopedic · 69d
Cleared Jul 23, 2002
ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM
K020356 · MNH
Orthopedic · 169d
Cleared Apr 26, 2000
DELTALOC ANTERIOR CERVICAL PLATE SYSTEM
K993513 · KWQ
Orthopedic · 191d
Cleared Jan 03, 2000
ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD
K993873 · KTT
Orthopedic · 49d
Cleared Sep 22, 1999
PYLON INTRAMEDULLAARY NAIL SYSTEM
K992350 · HSB
Orthopedic · 70d
Cleared May 22, 1998
ALPHATEC WIRE EXTERNAL FIXATION SYSTEM
K980788 · JDW
Orthopedic · 81d
Cleared Apr 28, 1997
ALPHATEC EXTERNAL FIXATION SYSTEM
K964400 · KTT
Orthopedic · 175d
Cleared Feb 14, 1996
MIRAGE SPINAL SYSTEM FOR SEVERE SPONDYLOLISTHESIS
K951846 · KWP
Orthopedic · 300d
Cleared Sep 28, 1994
ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW
K926417 · KTT
Orthopedic · 644d
Cleared Jun 29, 1994
ALPHA SPINAL SYSTEM
K930515 · KWP
Orthopedic · 513d
Cleared Feb 17, 1994
ALPHATEC COMPRESSION AND RECONSTRUCTION PLATES
K933112 · HRS
Orthopedic · 237d
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