Biocellect -Perio
FDA 510(k) K020396 · Imtec Corp.
510(k) numberK020396
Submission
- Device name
- Biocellect -Perio
- Applicant
- Imtec Corp.
Ardmore, OK, US - Received
- February 6, 2002
- Decision date
- April 10, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- LYC – Bone Grafting Material, Synthetic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 872.3930
- Specialty
- Dental
- Implant
- Yes
A synthetic bone grafting material is synthetically-derived device, such as hydroxylapatite, intended to fill, augment, or reconstruct periodontal and or bony defects of the upper or lower jaw.
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Questions and answers
When was Biocellect -Perio cleared by the FDA?
Biocellect -Perio (K020396) received a 510(k) decision of Substantially Equivalent on April 10, 2002, 63 days after the submission was received.
What is the product code of K020396?
The FDA product code is LYC – Bone Grafting Material, Synthetic, a Class II (moderate risk) device regulated under 21 CFR 872.3930.