ORTHOMET LHMC FEMORAL STEM— 510(k) K931678

Substantially Equivalent

Orthomet, Inc.

FDA 510(k) clearance K931678 for ORTHOMET LHMC FEMORAL STEM, Substantially Equivalent on 1994-10-14. Applicant: Orthomet, Inc.. Device class: 2.

Clearance details

Applicant: Orthomet, Inc.
Product code: Code HMC
Device class: Class 2
Regulation: 21 CFR 886.1510
Advisory panel: Ophthalmic
Date received: 1993-04-06
Decision date: 1994-10-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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K945783 — ORTHOMET TITANIUM HYBRID FEMORAL STEM1995-05-30
K943873 — ORTHOMET ANATOMICALLY GUIDED CARPAL TUNNEL RELEASE SY1995-04-26
K944752 — ORTHOMET RESURFACING FEMORAL COMPONENT1994-12-28
K930771 — PERFECTA TOTAL HIP SYSTEM COATED COCR FEMORAL STEM1994-11-30

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