KNEE AID— 510(k) K760002
Substantially EquivalentZimmer, Inc.
FDA 510(k) clearance K760002 for KNEE AID, Substantially Equivalent on 1976-07-26. Applicant: Zimmer, Inc.. Device class: 1.
Clearance details
- Applicant
- Zimmer, Inc.
- Product code
- Code IQI
- Device class
- Class 1
- Regulation
- 21 CFR 890.3475
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- 1831 Olive St. St. Louis, MO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.