FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO

K Number: K894959 · Decision Sep 14, 1990
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
84
Applicant Total
20
Review Days
403

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Basic Information

Device Name
CYPRESS CERVICAL TRACTION EQUIPMENT, CYPRESS HALO
K Number
K894959
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Alphatec Mfg., Inc.
Date Received
August 7, 1989
Decision Date
September 14, 1990
Product Code
JEC
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JEC Component, Traction, Invasive

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Other Clearances by Alphatec Mfg., Inc.

K Number Device Name
K033090 ICON POLYAXIAL PEDICLE SCREW SYSTEM
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K020356 ALPHA MIRAGE TOP TIGHTENING SPINAL SYSTEM
K993513 DELTALOC ANTERIOR CERVICAL PLATE SYSTEM
K993873 ALPHATEC EXTERNAL FIXATION SYSTEM COMPRESSION/DISTRACTION ROD
K992350 PYLON INTRAMEDULLAARY NAIL SYSTEM
K980788 ALPHATEC WIRE EXTERNAL FIXATION SYSTEM
K964400 ALPHATEC EXTERNAL FIXATION SYSTEM
K951846 MIRAGE SPINAL SYSTEM FOR SEVERE SPONDYLOLISTHESIS
K926417 ALPHATEC 130-150 SLOTTED COMPRESSION HIP SCREW
Search all 20 clearances from Alphatec Mfg., Inc. →