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

EXTREMITY BONE SCREW

K Number: K963118 · Decision Oct 10, 1996
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
43
Review Days
59

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Basic Information

Device Name
EXTREMITY BONE SCREW
K Number
K963118
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Acu Med, Inc.
Date Received
August 12, 1996
Decision Date
October 10, 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 Acu Med, Inc.

K Number Device Name
K021321 WRIST FUSION PLATE
K013616 POLARUS CAP SCREW
K012655 CONGRUENT BONE PLATE SYSTEM
K992525 ACUMED MODULAR SHOULDER SYSTEM
K993657 ACUMED SUTURE ANCHOR
K980103 ACUMED SUTURE ANCHOR
K965028 ACUMED SUTURE WASHER
K965029 STABLELOC II EXTERNAL FIXATOR
K964500 ACUMED TENSION BAND PIN
K963026 TBD
Search all 43 clearances from Acu Med, Inc. →