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

HAMMERLOCK 2

K Number: K133520 · Decision Jan 9, 2014
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
10
Review Days
55

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Basic Information

Device Name
HAMMERLOCK 2
K Number
K133520
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomedical Enterprises, Inc.
Date Received
November 15, 2013
Decision Date
January 9, 2014
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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Other Clearances by Biomedical Enterprises, Inc.

K Number Device Name
K153573 Converge
K150125 Elite Nitinol Fixation System
K143023 Nitinol Compression Plating System
K142292 Speed, Speed Shift, Speed Titan, Speed Arc
K133270 SPEED ARC
K124022 SPEED SHIFT
K061385 OSSTAPLE, OSSPLATE, OSSFORCE
K023486 OSSTAPLE, MAXILLOFACIAL
K023488 OSSTAPLE, CRANIOFACIAL