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

MEDICINELODGE, INC. SET SCREW

K Number: K961905 · Decision Aug 6, 1996
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
8
Review Days
82

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Basic Information

Device Name
MEDICINELODGE, INC. SET SCREW
K Number
K961905
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medicinelodge, Inc.
Date Received
May 16, 1996
Decision Date
August 6, 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

Other 510(k) clearances with the same product code (HWC), ordered by most recent decision date.

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Other Clearances by Medicinelodge, Inc.

K Number Device Name
K072525 ZIPKNOT, MODEL 1017-3000
K051488 MEDICINELODGE ZIPKNOT
K962705 MLI MODULAR STAPLE
K961920 CROSS PIN
K962194 MLI SOFT TISSUE SCREW & WASHER SYSTEM
K961025 EXPANDED BODY SUTURE
K953350 MLI INTERFERENCE SCREW