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HXP — Instrument, Bending Or Contouring Class I

FDA Device Classification

Classification Details

Product Code
HXP
Device Class
Class I
Regulation Number
888.4540
Submission Type
Review Panel
OR
Medical Specialty
Orthopedic
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K872858ace medicalWILLIAMS VERTEBRAL SPREADEROctober 15, 1987
K800733stainless mfgDOUBLE-EDGE CURETTEApril 8, 1980
K800731stainless mfgMENISCAL SAWApril 8, 1980
K800732stainless mfgMENISCOTOMEApril 8, 1980
K800730stainless mfgRETROGRADE KNIFEApril 8, 1980