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

PM CEMENTLESS SCREW-IN ACETABULAR CUP

K Number: K850773 · Decision May 2, 1985
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
22
Review Days
66

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Basic Information

Device Name
PM CEMENTLESS SCREW-IN ACETABULAR CUP
K Number
K850773
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Advanced Biosearch Assn.
Date Received
February 25, 1985
Decision Date
May 2, 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)

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K855030 CHAMPY BONE PLATES & BONE SCREWS
K855031 MANUAL SURGICAL INSTRUMENTS & ACCESS.CHAMPY BONE P
K853916 P.M. HIP-FEMORAL PROSTHESIS
K852839 FREEMAN HIP
K853418 SAFTI-BRACELET
K852517 CLS HIP PROSTHESIS
K852699 FREEMAN ACETABULAR CUP
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