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

LMT BONE ANCHOR

K Number: K951472 · Decision Jul 3, 1995
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
1040
Applicant Total
17
Review Days
95

Basic Information

Device Name
LMT BONE ANCHOR
K Number
K951472
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
LI MEDICAL TECHNOLOGIES, INC.
Date Received
March 30, 1995
Decision Date
July 3, 1995
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

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Other Clearances by LI MEDICAL TECHNOLOGIES, INC.

K Number Device Name
K002413 ULTRASORB SUTURE ANCHOR
K993373 ROTORBLADE SUTURE ANCHOR
K992938 ROTORBLADE SUTURE ANCHOR
K983435 ROTORBLADE
K981755 LM ANCHOR
K981764 LM ANCHOR
K963288 LM BONE ANCHOR
K963812 LM BONE ANCHOR (ORTHOPEDICS)
K960825 LM ANCHOR OR OTHER PROPRIETARY NAME
K960439 LM BONE ANCHOR
Search all 17 clearances from LI MEDICAL TECHNOLOGIES, INC. →