HWB — Extractor Class I

FDA Device Classification

FDA product code HWB covers "Extractor", a Class I medical device regulated under 21 CFR 888.4540. Submissions are reviewed by the Orthopedic panel. At least 5 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
HWB
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
K873710ArthropedicsMAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350Nov 2, 1987
K870844Warsaw OrthopedicSCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTORMar 13, 1987
K870083Terray ManufacturingFERRAY EXTRACTORFeb 26, 1987
K801327Anspach EffortTHE EXTRACTOR I TMJun 9, 1980
K780300Richard Medical EquipHIP PLATE REMOVAL INSTRUMENTFeb 28, 1978