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Cleared by FDA 510(k) INNESIS PEEK TL Cage
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- 510(k) Number: K140577
- Trade/ Device Name: INNESIS PEEK TL Cage
- Regulation Number: 21 CFR 888.3080
- Regulation Name: Intervertebral body fusion device
- Regulatory Class: Class II
- Product Code: MAX
PERV
Cleared by FDA 510(k) INNESIS PEEK Cervical Cage
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