BIOMET CONCENTRIC HEX SCREW— 510(k) K781389
Substantially EquivalentBiomet, Inc.
FDA 510(k) clearance K781389 for BIOMET CONCENTRIC HEX SCREW, Substantially Equivalent on 1978-08-21. Applicant: Biomet, Inc.. Device class: 2.
Clearance details
- Applicant
- Biomet, Inc.
- Product code
- Code JDO
- Device class
- Class 2
- Regulation
- 21 CFR 888.3030
- Advisory panel
- Orthopedic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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More clearances from Biomet, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.