Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K053228 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Bone Void Filler, sterile orthopedic product, 510 (k) #K053228. The product is delivered in a syrin... | 2 | 11/01/2010 |
FEI # 3002498892 Theken Spine Llc |
| FormPutty Bone Void Filler 10cc The product is sealed in a foil pouch and then placed in a box fo... | 3 | 09/18/2008 |
FEI # 3002498892 Theken Spine LLC |
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