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

HIPLOC COMPRESSION HIP SCREW

K Number: K080685 · Decision Aug 15, 2008
Classifications
1
FEI Numbers
61
Registration Numbers
61
Same Product Code
22
Applicant Total
32
Review Days
157

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Basic Information

Device Name
HIPLOC COMPRESSION HIP SCREW
K Number
K080685
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Manufacturing, Inc.
Date Received
March 11, 2008
Decision Date
August 15, 2008
Product Code
JDO
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
JDO Device, Fixation, Proximal Femoral, Implant

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Other Clearances by Biomet Manufacturing, Inc.

K Number Device Name
K130390 COMPREHENSIVE CONVERTIBLE GLENOID
K113271 METAL-ON-METAL HIP SYSTEMS-ADDITIONAL CONTRAINDICATIONS
K113121 COMPREHENSIVE REVERSE SHOULDER
K080088 BIOMET SPORTS MEDICINE ANCHOR DEVICES AND ZIPLOOP CONSTRUCTS
K071271 BIOMET CABLE SYSTEM
K070399 100KGY E-POLY ACETABULAR LINERS-ADDITIONAL PROFILES
K063515 TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE
K061340 23 MM SINGLE-PEG PATELLA COMPONENT
K061433 VANGUARD ANATOMIC PATELLA GROOVE (APG) / VANGUARD V GROOVE
K053505 REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS
Search all 32 clearances from Biomet Manufacturing, Inc. →