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U.S. Department of Health and Human Services

Product Classification
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Device accessories, fixation, spinal interlaminal
Regulation Description Spinal interlaminal fixation orthosis.
Regulation Medical Specialty Orthopedic
Review Panel Orthopedic
Product CodeLYP
Premarket Review Spinal Devices (DHT6B)
Spinal Devices (DHT6B)
Submission Type 510(k)
Regulation Number 888.3050
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting		 Eligible
Implanted Device? Yes
Life-Sustain/Support Device? No
Recognized Consensus Standards
Third Party Review Not Third Party Eligible
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