510(k) K802838
K802838 is an FDA 510(k) premarket notification submitted by Amsco Co. for the device "STERNUM SAW BLADE". The FDA issued a decision of Substantially Equivalent on December 11, 1980. The device falls under product code GFA (Blade, Saw, General & Plastic Surgery, Surgical), a Class I device regulated under 21 CFR 878.4820. Amsco Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 11, 1980
- Date Received
- November 12, 1980
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Blade, Saw, General & Plastic Surgery, Surgical
- Device Class
- Class I
- Regulation Number
- 878.4820
- Review Panel
- SU
- Submission Type