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

TITANIUM CANNULATED INTERFERENCE SCREW

K Number: K021030 · Decision Jun 25, 2002
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
12
Review Days
88

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Basic Information

Device Name
TITANIUM CANNULATED INTERFERENCE SCREW
K Number
K021030
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Future Medical Systems, Inc.
Date Received
March 29, 2002
Decision Date
June 25, 2002
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 Future Medical Systems, Inc.

K Number Device Name
K023963 ADHOC CLAW
K013685 PLLA CANNULATED INTERFERENCE SCREW
K002040 FMS SOLO
K980808 ENDO FMS UROLOGY
K955500 FMS ARTHOPROBE
K954465 FMS DUO
K954217 ARTHROPLAST & ARTHRO-CUTTER
K951843 REF. 4102CV INTERMEDIARY TUBING, REF. 4509CV STERILE ZONE KIT
K951702 FMS HIGH FLOW ARTHRO-SHEATH
K951701 FMS ARTHRO-CUTTER
Search all 12 clearances from Future Medical Systems, Inc. →