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

POLYMER THREADED ANCHOR / SUTURE COMBINATION

K Number: K982963 · Decision Nov 20, 1998
Classifications
1
FEI Numbers
227
Registration Numbers
227
Same Product Code
562
Applicant Total
11
Review Days
88

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Basic Information

Device Name
POLYMER THREADED ANCHOR / SUTURE COMBINATION
K Number
K982963
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3350
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthopaedic Biosystems, Ltd.
Date Received
August 24, 1998
Decision Date
November 20, 1998
Product Code
JDI
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
JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

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Other Clearances by Orthopaedic Biosystems, Ltd.

K Number Device Name
K000797 OBL 2.0 MM MINI TAC ANCHOR, MODEL 10-1629-01
K982996 POLYMER OBL SB ANCHOR / SUTURE COMBINATION
K983169 POLYMER THREADED ANCHOR
K972326 PEBA ANCHOR/SUTURE COMBINATION
K963420 CANCELLOUS SCREW WASHER
K963432 GUIDE WIRES FOR CANNULATED SCREWS
K963433 THREADED FIXATION PIN
K962779 COMPRESSION SCREW
K951451 PEBA ANCHOR (MULTIPLE SIZES)
K942889 SB ANCHOR
Search all 11 clearances from Orthopaedic Biosystems, Ltd. →