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

FASICULATED NAIL

K Number: K861365 · Decision May 6, 1986
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
42
Review Days
25

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Basic Information

Device Name
FASICULATED NAIL
K Number
K861365
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Lake Region Mfg., Inc.
Date Received
April 11, 1986
Decision Date
May 6, 1986
Product Code
HSB
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
HSB Rod, Fixation, Intramedullary And Accessories

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Other Clearances by Lake Region Mfg., Inc.

K Number Device Name
K092965 TRAILRUNNER GUIDEWIRES
K082922 FREEWAY AND RAILRUNNER GUIDEWIRES
K081708 TAXI ENDOSCOPIC GUIDEWIRE
K080144 MANDREL GUIDEWIRES OR M-WIRES
K073655 PEGASUS STEERABLE (PTCA) GUIDEWIRE
K060454 TITAN GUIDEWIRE
K052347 TITAN STEERABLE (PTCA) GUIDEWIRE
K042338 CORONARY PERIPHERAL AND RENAL STEERABLE GUIDEWIRE
K041624 PTCA STEERABLE HYDROPHILIC GUIDEWIRE
K040825 LAKE REGION HYDROPHILIC GUIDEWIRE
Search all 42 clearances from Lake Region Mfg., Inc. →