FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

TITANIUM MITTELMEIER TYPE ACETABULAR

K Number: K842466 · Decision Jan 30, 1985
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
6
Review Days
219

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Basic Information

Device Name
TITANIUM MITTELMEIER TYPE ACETABULAR
K Number
K842466
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
American Ortomed Corp.
Date Received
June 25, 1984
Decision Date
January 30, 1985
Product Code
KWA
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
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

Similar 510(k) Clearances

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

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Other Clearances by American Ortomed Corp.

K Number Device Name
K842518 UNILOC-CEMENTLESS & SELF TAP ACETABULAR
K842465 UNILOC
K840413 CEMENT RESTRICTOR
K820719 THE ICR KNEE
K780497 SPHERISTEM TOTAL HIP PROSTHESIS