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

LIDGRER-LUND ACETABULAR SOCKETS

K Number: K852369 · Decision Jun 18, 1985
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
44
Applicant Total
21
Review Days
14

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Basic Information

Device Name
LIDGRER-LUND ACETABULAR SOCKETS
K Number
K852369
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3320
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Link America, Inc.
Date Received
June 4, 1985
Decision Date
June 18, 1985
Product Code
JDL
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
JDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)

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K914804 RADIUS OSTEOTOMY PLATES
K914803 SCHWABE RADIUS PLATES
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