510(k) K770059
K770059 is an FDA 510(k) premarket notification submitted by Robert R. Moore for the device "ORTHOPEDIC SPECIALTIES". The FDA issued a decision of Substantially Equivalent on Jan 14, 1977. Robert R. Moore has at least 4 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 14, 1977
- Date Received
- Jan 11, 1977
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No