FDA 510(k) FDA class 2 Unknown 🇺🇸 United States

SILKON TITANIUM CABLE SYSTEM

K Number: K942300 · Decision Jan 9, 1995
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
128
Applicant Total
14
Review Days
242

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Basic Information

Device Name
SILKON TITANIUM CABLE SYSTEM
K Number
K942300
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3010
Medical Specialty
Orthopedic
Decision
Unknown
Statement or Summary
Summary
Applicant
American Medical Electronics, Inc.
Date Received
May 12, 1994
Decision Date
January 9, 1995
Product Code
JDQ
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
JDQ Cerclage, Fixation

Similar 510(k) Clearances

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Other Clearances by American Medical Electronics, Inc.

K Number Device Name
K951232 EXPANDED RANGE OF SUTURE SIZES OGDEN ANCHORS: 7.4MM AND 5.5MM
K952348 OGDEN ANCHOR
K950875 OGDEN ANCHOR
K951493 OGDEN ANCHOR
K951545 OGDEN ANCHOR FOR ALL ORTHOPAEDIC SOFT TISSUE APPLICATIONS
K941029 OGDEN ANCHOR-SMALL (TENTATIVE)
K931381 AME UNIVERSAL FIXATION SYSTEM
K935065 OGDEN ANCHOR ADDITIONAL APPLICATIONS
K935167 OGDEN ANCHOR (MODIFICATION)
K932687 AME(R) UNIVERSIAL CABLE SYSTEM
Search all 14 clearances from American Medical Electronics, Inc. →