510(k) K912761
K912761 is an FDA 510(k) premarket notification submitted by Blairden Precision Instruments, Inc. for the device "SURGICAL SAW BLADES". The FDA issued a decision of Substantially Equivalent on July 19, 1991. The device falls under product code GFA (Blade, Saw, General & Plastic Surgery, Surgical), a Class I device regulated under 21 CFR 878.4820. Blairden Precision Instruments, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 19, 1991
- Date Received
- June 24, 1991
- 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