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

LINK, ACETABULAR REVISION MESH CUP

K Number: K972760 · Decision Oct 22, 1997
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
6
Applicant Total
21
Review Days
90

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Basic Information

Device Name
LINK, ACETABULAR REVISION MESH CUP
K Number
K972760
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Link America, Inc.
Date Received
July 24, 1997
Decision Date
October 22, 1997
Product Code
JDJ
Advisory Committee
General, Plastic Surgery
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
JDJ Mesh, Surgical, Acetabular, Hip, Prosthesis

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Other Clearances by Link America, Inc.

K Number Device Name
K964458 ELLIS EXTERNAL MINI-FIXATOR SYSTEM
K955296 LINK MP RECONSTRUCTION HIP
K954186 SLED UNICOMPARTMENT KNEE SYSTEM
K931571 LINK CERAMIC HEADS 12/14 X 32MM
K931572 LINK CERAMIC HEADS 14/16 X 32MM
K920756 FELDMUHLE CERAMIC HEAD
K914804 RADIUS OSTEOTOMY PLATES
K914803 SCHWABE RADIUS PLATES
K895507 LINK GIEBEL BLADE PLATE SYSTEM
K873507 LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM
Search all 21 clearances from Link America, Inc. →