510(k) K042332
K042332 is an FDA 510(k) premarket notification submitted by Fournitures Hospitalieres Industrie for the device "TITANIUM TELEGRAPH HUMERAL NAIL". The FDA issued a decision of Substantially Equivalent on Oct 7, 2004. The device falls under product code HSB (Rod, Fixation, Intramedullary And Accessories), a Class II device regulated under 21 CFR 888.3020. Fournitures Hospitalieres Industrie has 23 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 7, 2004
- Date Received
- Aug 30, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Rod, Fixation, Intramedullary And Accessories
- Device Class
- Class II
- Regulation Number
- 888.3020
- Review Panel
- OR
- Submission Type
- 510(k)