ENHANCED MODULAR AUSTIN MOORE HIP— 510(k) K936044
Substantially EquivalentZimmer, Inc.
FDA 510(k) clearance K936044 for ENHANCED MODULAR AUSTIN MOORE HIP, Substantially Equivalent on 1994-04-26. Applicant: Zimmer, Inc.. Device class: 2.
Clearance details
- Applicant
- Zimmer, Inc.
- Product code
- Code KMC
- Device class
- Class 2
- Regulation
- 21 CFR 888.3340
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warsaw, IN, US
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Recalls naming K936044
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K936044.
Data sourced from openFDA. This site is unofficial and independent of the FDA.