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

SB ANCHOR

K Number: K942889 · Decision Aug 25, 1995
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
11
Review Days
431

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Basic Information

Device Name
SB ANCHOR
K Number
K942889
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Orthopaedic Biosystems, Ltd.
Date Received
June 20, 1994
Decision Date
August 25, 1995
Product Code
JDR
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
JDR Staple, Fixation, Bone

Similar 510(k) Clearances

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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
K982963 POLYMER THREADED ANCHOR / SUTURE COMBINATION
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)
Search all 11 clearances from Orthopaedic Biosystems, Ltd. →