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

COMPRESSION SCREW

K Number: K962779 · Decision Aug 23, 1996
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
11
Review Days
37

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Basic Information

Device Name
COMPRESSION SCREW
K Number
K962779
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Orthopaedic Biosystems, Ltd.
Date Received
July 17, 1996
Decision Date
August 23, 1996
Product Code
HWC
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
HWC Screw, 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
K951451 PEBA ANCHOR (MULTIPLE SIZES)
K942889 SB ANCHOR
Search all 11 clearances from Orthopaedic Biosystems, Ltd. →