FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE

K Number: K821024 · Decision May 14, 1982
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
18
Applicant Total
373
Review Days
31

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Basic Information

Device Name
DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE
K Number
K821024
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4760
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Howmedica Corp.
Date Received
April 13, 1982
Decision Date
May 14, 1982
Product Code
GDT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GDT Staple, Removable (Skin)

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Other Clearances by Howmedica Corp.

K Number Device Name
K983528 MICRO DYNAMIC MESH
K983404 TYPE 3 FEMORAL COMPONENTS
K980925 DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATION
K980926 DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATION
K980632 DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION
K980626 DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATION
K983419 HOFFMANN II MIAMI POST
K982958 ZETA MULTIZONE LOCKING NAIL SYSTEM
K982873 ZETA MULTIZONE SCN LOCKING NAIL
K982531 HOWMEDICA LEIBINGER RESORBABLE FIXATION SYSTEM
Search all 373 clearances from Howmedica Corp. →