510(k) K050767
K050767 is an FDA 510(k) premarket notification submitted by Regeneration Technologies, Inc. for the device "STERLING INTERFERENCE SCREW ST". The FDA issued a decision of Substantially Equivalent on June 9, 2005. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Regeneration Technologies, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 9, 2005
- Date Received
- March 25, 2005
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Screw, Fixation, Bone
- Device Class
- Class II
- Regulation Number
- 888.3040
- Review Panel
- OR
- Submission Type