510(k) K830720
K830720 is an FDA 510(k) premarket notification submitted by Acufex Microsurgical, Inc. for the device "GRAF MENISCAL SUTURE SET". The FDA issued a decision of Substantially Equivalent on June 16, 1983. The device falls under product code FZX (Guide, Surgical, Instrument), a Class I device regulated under 21 CFR 878.4800. Acufex Microsurgical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 16, 1983
- Date Received
- March 8, 1983
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Guide, Surgical, Instrument
- Device Class
- Class I
- Regulation Number
- 878.4800
- Review Panel
- SU
- Submission Type