# K050357: Camceram TCP

- Pathway: 510(k) (Abbreviated)
- Applicant: Cam Implants B.V.
- Decided: Apr 21, 2005 after 66 days
- Product code: MQV (Filler, Bone Void, Calcium Compound)
- Device class: 2
- Regulation: 21 CFR 888.3045
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K990131 (1999). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K994337: Vitoss Scaffold Synthetic Cancellous Bone Void Filler, Orthovita Co. (2000) Summary page 1.
- K014053: Conduit TCP Granules, Depuyacromed (2002) Summary page 1.

## Most influential descendants
- K102937: Osteophil Beta-TCP (2010), 0 descendants of its own

## Indications for use
CAMCERAM TCP is a bone void filler is a resorbable implant intended to fill bony void or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.

Source page: https://510kreport.com/device/K050357
Methodology: https://510kreport.com/methodology