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

BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED

K Number: K925682 · Decision Jan 7, 1994
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
41
Review Days
427

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Basic Information

Device Name
BIOPRO ZIRALLOY MODULAR FEMORAL HEADS, MODIFIED
K Number
K925682
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Biopro, Inc.
Date Received
November 6, 1992
Decision Date
January 7, 1994
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

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Other Clearances by Biopro, Inc.

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K130298 BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM
K121973 BIOPRO HEMI-EDGE TOE SYSTEM
K100761 BIOPRO POLAR HEAD
K101030 MODIFICATION TO HBS HEADLESS BONE SCREW
K090208 BIOPRO FEMORAL HEADS
K083490 BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685
K082705 BIOPRO BIPOLAR HEAD, MODELS 18130-18152
Search all 41 clearances from Biopro, Inc. →