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

OGDEN ANCHOR

K Number: K950875 · Decision Jul 11, 1995
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
14
Review Days
133

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Basic Information

Device Name
OGDEN ANCHOR
K Number
K950875
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
American Medical Electronics, Inc.
Date Received
February 28, 1995
Decision Date
July 11, 1995
Product Code
HWC
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HWC), ordered by most recent decision date.

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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
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
K942300 SILKON TITANIUM CABLE SYSTEM
K935167 OGDEN ANCHOR (MODIFICATION)
K932687 AME(R) UNIVERSIAL CABLE SYSTEM
Search all 14 clearances from American Medical Electronics, Inc. →