510(k) K761206
K761206 is an FDA 510(k) premarket notification submitted by Smith & Nephew, Mpl Division for the device "INTEROSSEOUS NEEDLE". The FDA issued a decision of Substantially Equivalent on December 13, 1976. The device falls under product code DZM (Needle, Dental), a Class I device regulated under 21 CFR 872.4730. Smith & Nephew, Mpl Division has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 13, 1976
- Date Received
- December 7, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Dental
- Device Class
- Class I
- Regulation Number
- 872.4730
- Review Panel
- DE
- Submission Type